Online CDR Medical/Disability Terms

Below is a listing of medical/disability terms used in our database.

11;22 TRANSLOCATION (PARTIAL TRISOMY 11;22)
11Q SYNDROME (JACOBSEN SYNDROME, DELETION ON LONG ARM OF CHROMOSOME 11)
18P- SYNDROME (18 P MINUS, SHORT ARM 18 DELETION, CHROMOSOME 18, MONOSOMY 18P)
18Q- SYNDROME (18 Q MINUS, CHROMOSOME 18 LONG ARM DELETION)
4Q- SYNDROME (4 Q MINUS)
4Q2 & 3 TRISOMY
8P DUPLICATION (CHROMOSOME 8P DISORDER)
AARSKOG SYNDROME
ABDOMINAL MIGRAINE
ABDOMINAL PAIN
ABSENCE OF FINGERS - CONGENITAL (COMPLETE OR PARTIAL)
ACADEMICALLY GIFTED/TALENTED
ACHALASIA
ACHONDROGENESIS (NEONATAL DWARFISM,HYPOCHONDROGENESIS,LETHAL OSTEOCHONDRODYSPLAS
ACHONDROPLASIA/ DWARFISM
ACHROMATOPSIA (ROD MONOCHROMACY, BLUE CONE MONOCHROMACY)
ACID MALTASE DEFICIENCY (AMD, GLYCOGEN STORAGE DISEASE TYPE II, POMPE DISEASE)
ACIDEMIA, PROPIONIC
ACIDOSIS / ACIDEMIA
ACOUSTIC NEUROMA
ACQUIRED APHASIA
ACQUIRED IMMUNE DEFICIENCY SYNDROME (AIDS, UNSPECIFIED)
ACQUIRED SYPHILIS
ACRODERMATITIS ENTEROPATHICA
ACTH DEFICIENCY
ACUTE BRONCHIOLITIS
ACUTE LYMPHOCYTIC LEUKEMIA (ACUTE LYMPHOBLASTIC LEUKEMIA)
ACUTE MYELOID LEUKEMIA (AML)
ADAMS-OLIVER SYNDROME
ADDISON DISEASE (ADDISON-SCHILDER DISEASE)
ADOLESCENCE (TEEN/ADOLESCENT)
ADRENAL HYPOPLASIA (ADRENAL GLAND)
ADRENOCORTICAL INSUFFICIENCY SYNDROME/CONGENITAL ADRENAL HYPERPLASIA
ADRENOLEUKODYSTROPHY (ALD, ADDISON-SCHILDER, SUDANOPHILIC, ADRENOMYELONEUROPATHY, ETC.)
ADULT RESPIRATORY DISTRESS SYNDROME (ARDS, WET LUNG)
AGAMMAGLOBULINEMIAS, PRIMARY (ANTIBODY,GAMMAGLOBULIN,IMMUNOGLOBULIN DEFICIENCY)
AGENESIS OF THE CORPUS CALLOSUM
AGGRESSIVE BEHAVIOR
AGNOSIA (TACTILE)
AICARDI SYNDROME ( AGENESIS OF THE CORPUS CALLOSUM-CHORIORETINAL ABNORMALITY)
ALAGILLE SYNDROME (AHD)
ALBINISM
ALCOHOL ABUSE/ADDICTION/ALCOHOLISM
ALEXANDER'S DISEASE (A LEUKODYSTROPHY)
ALKAPTONURIA (ALCAPTONURIA, HOMOGENISTIC ACID OXIDASE DEFICIENCY, OCHRONOSIS)
ALL DISABLITIES/ ANY DISABILITY
ALLERGIC RHINITIS
ALLERGIES/ALLERGIC DISORDERS
ALOPECIA AREATA
ALPERS DISEASE
ALPHA-1-ANTITRYPSIN DEFICIENCY
ALPORT SYNDROME (HEREDITARY NEPHRITIS, EPSTEIN SYNDROME)
ALTERNATING HEMIPLEGIA OF CHILDHOOD
ALVEOLAR CAPILLARY DYSPLASIA (ACD)
ALZHEIMER'S DISEASE
AMBLYOPIA
AMNIOTIC BANDS
AMPUTATION (SEE ALSO ORTHOPEDIC DISORDERS)
AMYOTROPHIC LATERAL SCLEROSIS (ALS, LOU GEHRIG'S DISEASE)
ANAPLASTIC ASTROCYTOMA (MALIGNANT GLIOMA)
ANAPLASTIC EPENDYMOMA (GLIOMA)
ANDROGEN INSENSITIVITY SYNDROME
ANENCEPHALY
ANGELMAN SYNDROME (HAPPY PUPPET)
ANIRIDIA
ANKYLOGLOSSIA (TONGUE-TIE)
ANKYLOSING SPONDYLITIS (STRUMPELL-MARIE DISEASE, RHEUMATOID SPONDYLITIS)
ANOMALIES OF BLADDER AND/OR URETHRA
ANOMALIES OF INTESTINE
ANOMALIES OF UNSPECIFIED CHROMOSOMES
ANOPHTHALMIA/MICROPHTHALMIA
ANOREXIA NERVOSA (EATING DISORDER)
ANTISOCIAL PERSONALITY DISORDER (ASP)
ANTLEY BIXLER SYNDROME (ABS)
ANXIETY DISORDERS
APERT SYNDROME
APLASIA CUTIS CONGENITA (CONGENITAL SCALP DEFECT)
APLASTIC ANEMIA (SEE ALSO HEMATOLOGIC DISORDERS)
APRAXIA (DYSPRAXIA, DEVELOPMENTAL, BUCCOFACIAL, VERBAL)
ARACHNOID CYSTS
ARACHNOIDITIS (ARACHNITIS, SEROUS CIRCUMSCRIBED MENINGITIS, SPINAL ARACHNOIDITIS
ARGININO SUCCINIC ACIDURIA (ARG. SUCCINASE DEFICIENCY, ARGININOSUCCINATE LYASE..
ARNOLD-CHIARI SYNDROME
ARTERIOVENOUS MALFORMATION (AVM)
ARTHRITIS (SEE ALSO ORTHOPEDIC DISORDERS)
ARTHROGRYPOSIS
ARTHROGRYPOSIS MULTIPLEX CONGENITA (AMC)
ASPERGER'S SYNDROME
ASTHMA (REACTIVE AIRWAY DISEASE, SEE ALSO LUNG DISORDERS)
ASTROCYTOMA (BENIGN, BRAIN TUMOR)
ATAXIA (LACK OF COORDINATION, MUSCULAR INCOORDINATION)
ATAXIA TELANGIECTASIA
ATAXIA WITH LACTIC ACIDOSIS, TYPE II (PYRUVATE CARBOXYLASE (PC) DEFICIENCY
ATLANTO-AXIAL INSTABILITY AND OCCIPITAL-ATLANTAL INSTABLILITY (CRANIOVERTEBRAL INSTABILITY)
ATRESIA OF SMALL INTESTINE (DUODENUM, ILEUM, JEJUNUM)
ATRIAL FIBRILLATION (AF)
ATRIAL SEPTAL DEFECTS (ASD)
ATRIOVENTRICULAR SEPTAL (CANAL) DEFECT (AVSD)
ATTENTION DEFICIT DISORDER (ADD, HYPERACTIVITY, ADHD)
AUDITORY HALLUCINATIONS (HEARING VOICES)
AUDITORY NEUROPATHY
AUDITORY PROCESSING DISORDERS (APD, CAPD)
AUTISM (SEE ALSO DEVELOPMENTAL DELAY/DISABILITY)
AUTOIMMUNE INNER EAR DISEASE
AUTONOMIC NERVOUS SYSTEM DISORDERS
AUTOSOMAL DELETION SYNDROMES (UNSPECIFIED, MISSING OR PARTIAL CHROMOSOME)
BACTERIAL MENINGITIS
BARDET-BIEDL SYNDROME
BARRETT SYNDROME
BARTTER'S SYNDROME
BATTEN DISEASE (SPIELMEYER-VOGT, -MAYOU, -STENGEL, NEURONAL CEROID LIPOFUSCINOSES)
BATTERED WOMEN/DOMESTIC VIOLENCE
BEALS SYNDROME (CONTRACTURAL ARACHNODACTYLY)
BECKER MUSCULAR DYSTROPHY
BECKWITH-WIEDEMANN SYNDROME
BED-WETTING (NOCTURNAL ENURESIS)
BEHCET'S DISEASE (BEHCET'S SYNDROME)
BELL'S PALSY
BENIGN CONGENITAL HYPOTONIA (HYPOTONIA; MYONEURAL DISORDER)
BENIGN CONGENITAL MYOPATHY (CENTRAL CORE DISEASE, NEMALINE BODY DISEASE)
BENIGN ESSENTIAL TREMOR (FAMILIAL TREMOR, PRESENILE TREMOR SYNDROME)
BENIGN FAMILIAL HEMATURIA
BENIGN PAROXYSMAL POSITIONAL NYSTAGMUS (BPNN, CUPULOLITHIASIS)
BENIGN ROLANDIC EPILEPSY (BREC)
BEREAVEMENT (ADJUSTMENT REACTION)
BILATERAL RENAL AGENESIS (KIDNEY)
BILATERAL VERTICAL TALUS
BILIARY ATRESIA
BILIARY TRACT DISEASE (BILIARY DUCT, UNSPECIFIED)
BINSWANGER'S DISEASE
BIOTINIDASE DEFICIENCY
BIPOLAR DISORDER (MANIC DEPRESSION, MANIA)
BIRTH TRAUMA/DEFECTS
BIRTHMARKS (VASCULAR HAMARTOMAS, SKIN ANOMALIES)
BLACKFAN-DIAMOND (HYPOPLASTIC) ANEMIA
BLADDER CANCER (URINARY)
BLADDER DISEASE
BLEPHAROPHIMOSIS, PTOSIS, EPICANTHUS INVERSUS SYNDROME (BPES)
BLOOD (HEMATOLOGIC) DISORDERS
BLOOM SYNDROME (BLOOM-TORRE-MACKACEK SYNDROME)
BLOUNT'S DISEASE (TIBIA VARA)
BLUE RUBBER BLEB NEVUS
BONE MARROW TRANSPLANT
BORDERLINE PERSONALITY DISORDER
BOTULISM
BOWLEGS (CONGENITAL)
BRACHIAL PLEXUS INJURY
BRAIN STEM GLIOMA (M9380/3) (BRAIN TUMOR)
BRAIN TUMORS (SEE ALSO CANCER)
BRANCHIO-OTO-RENAL-SYNDROME (BOR, BRANCHIOOTIC, MELNICK-FRASER SYNDROME)
BREAST CANCER
BREATH-HOLDING SPELLS
BRONCHITIS
BRONCHOMALACIA
BRONCHOPULMONARY DYSPLASIA (BPD)
BROWN SYNDROME (TENDON SHEATH SYNDROME)
BRUCELLOSIS (BRUCELLA, BRUCELLEMIA)
BUERGER'S DISEASE (INFLAMMATORY OCCLUSIVE PERIPHERAL VASCULAR DISEASE)
BULIMIA (OVEREATING OF NONORGANIC ORIGIN, EATING DISORDER)
BULLYING
BURNS
CALCIFICATION IN BURSA OR IN TENDON (CALCIUM DEPOSITS)
CAMPTOMELIC SYNDROME (CAMPOMELIC DWARFISM, CAMPTOMELIC DWARFISM, CMDI)
CANAVAN'S DISEASE (A LEUKODYSTROPHY)
CANCER
CANCER OF THE CERVIX (CERVICAL CANCER)
CANCER OF THE LIVER (PRIMARY)
CARBOHYDRATE TRANSPORT/METABOLISM DISORDERS (OXALOSIS, HYPEROXALURIA, ETC.)
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE I (GLYCOSYLATION DISORDERS)
CARDIAC DYSRHYTHMIA (HEART RHYTHM DISORDER, BRADYCARDIA)
CARDIAC PACEMAKER (HEART)
CARDIO-FACIO-CUTANEOUS SYNDROME (CFC SYNDROME)
CARDIOMYOPATHY (IDIOPATHIC HYPERTROPHIC SUBAORTIC STENOSIS, IHSS, HCM)
CARNEY SYNDROME (CARNEY COMPLEX)
CARNITINE PALMITYL TRANSFERASE DEFICIENCY (CPTD)
CARNOSINEMIA (CARNOSINASE DEFICIENCY)
CARPAL TUNNEL SYNDROME (REPETITIVE MOTION SYNDROME)
CARPENTER'S SYNDROME (ACROCEPHALOPOLYSYNDACTYLY, ACPS TYPE II)
CASTLEMAN'S DISEASE (LYMPH NODE HYPERPLASIA, CASTLEMAN TUMOR)
CAT-SCRATCH DISEASE (CAT-SCRATCH FEVER, PARINAUD'S SYNDROME)
CATAPLEXY
CATARACTS
CAUDAL SYNDROME (CAUDAL DYSPLASIA, SACRAL REGRESSION, SACRAL AGENESIS)
CAYLER SYNDROME (ASYMMETRIC CRYING FACIES WITH CARDIAC DEFECTS)
CELIAC SPRUE
CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL (ONDINE'S CURSE)
CEREBELLAR AGENESIS
CEREBELLAR ASTROCYTOMA (CEREBELLUM, BRAIN TUMOR)
CEREBRAL ASTROCYTOMA (CEREBRUM, BRAIN TUMOR)
CEREBRAL LIPIDOSES (NEURONAL LIPOFUSCINOSES, NCL, CEROID LIPOFUSCINOSIS)
CEREBRAL PALSY (CP) (SEE ALSO DEV DELAY/DISABIL, ORTHOPEDIC DISORDERS)
CEREBRAL-OCULAR-FACIAL SKELETAL SYNDROME (COFS)
CEREBROCOSTOMANDIBULAR SYNDROME (RIB GAP DEFECTS WITH MICROGNATHIA)
CEREBROVASCULAR ACCIDENT (CVA)
CHARCOT-MARIE-TOOTH SYNDROME / PERONEAL MUSCULAR ATROPHY
CHARGE ASSOCIATION (CHARGE SYNDROME)
CHIARI-FROMMEL SYNDROME
CHICKEN POX (VARICELLA, UNSPECIFIED COMPLICATIONS)
CHILD ABUSE/NEGLECT
CHILDHOOD ATAXIA WITH CENTRAL HYPOMYELINATION (CACH)
CHILDHOOD DISINTEGRATIVE DISORDER (CDD, HELLER'S SYNDROME)
CHILDHOOD GENDER IDENTITY DISORDER (GID)
CHLAMYDIA TRACHOMATIS
CHOLANGITIS (PRIMARY SCLEROSING)
CHONDRODYSPLASIA PUNCTATA ( RHIZOMELIC )
CHROMOSOMAL ANOMALIES (GENERAL)
CHROMOSOME 10, DISTAL TRISOMY 10Q
CHROMOSOME 10, MONOSOMY10P (10P DELETION SYNDROME-PARTIAL)
CHROMOSOME 10Q (DELETION)
CHROMOSOME 12 DISORDERS
CHROMOSOME 13 PARTIAL MONOSOMY 13Q (13Q- SYNDROME,13 Q MINUS)
CHROMOSOME 1Q- (1 Q MINUS)
CHROMOSOME 22 RING
CHROMOSOME 22, TRISOMY MOSAIC
CHROMOSOME 3, MONOSOMY 3P2
CHROMOSOME 3, TRISOMY 3Q2 (PARTIAL TRISOMY 3Q SYNDROME, DISTAL 3Q2 DUPLICATION))
CHROMOSOME 5, TRISOMY 5P
CHROMOSOME 8 DISORDERS (MOSAIC TRISOMY 8)
CHRONIC FATIGUE IMMUNE DYSFUNCTION SYNDROME (CFIDS,EPSTEIN-BARR VIRUS)
CHRONIC GRANULOMATOUS DISEASE
CHRONIC ILLNESS (GENERAL)
CHRONIC ILLNESS / OTHER HEALTH IMPAIRED
CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY
CHRONIC LYMPHOCYTIC LEUKEMIA
CHRONIC MUCOID OTITIS MEDIA (GLUE EAR)
CHRONIC MYELOGENOUS LEUKEMIA
CHRONIC NEUTROPENIA SYNDROME
CHRONIC PAIN
CHRONIC PANCREATITIS
CHRONIC SPASMODIC DYSPHONIA (ABDUCTOR SPASTIC DYSPHONIA, CSD, DYSPHONIA SPASTICA
CHURG-STRAUSS SYNDROME (ALLERGIC GRANULOMATOUS ANGIITIS)
CITRULLINEMIA (CITRULLINURIA,ARGINASE DEFICIEN,ARGININOSUCCINIC ACID SYNTHETASE)
CLEFT LIP AND PALATE (SEE ALSO ORAL-FACIAL DISORDERS)
CLEIDOCRANIAL DYSTOSIS
CLOACA, PERSISTENT (ANORECTAL MALFORMATIONS, CLOACAL EXSTROPHY)
CLUBFOOT (SEE ALSO ORTHOPEDIC DISORDERS)
COARCTATION OF THE AORTA
COATS' DISEASE (EXUDATIVE RETINITS)
COCAINE USE (CRACK ADDICTION)
COCKAYNE SYNDROME
COFFIN LOWRY SYNDROME
COFFIN SIRIS SYNDROME (DWARFISM-ONYCHODYSPLASIA)
COGAN'S SYNDROME TYPE I
COHEN SYNDROME (PEPPER SYNDROME, HYPOTONIA-OBESITY-PROMINENT INCISORS SYNDROME, NORIO SYNDROME)
COLD ANTIBODY HEMOLYTIC ANEMIA (COLD AGGLUTININ DISEASE)
COLIC
COLOR BLINDNESS
COLORECTAL CANCER (CANCER OF THE COLON AND/OR RECTUM)
COLOSTOMY
COLOSTOMY AND ENTEROSTOMY COMPLICATION
COMMON COLD (ACUTE NASOPHARYNGITIS)
COMMON VARIABLE IMMUNODEFICIENCY (ACQUIRED HYPOGAMMAGLOBULINMIA)
COMMUNICATION DISORDERS
CONDUCT DISORDER
CONDYLOMA (GENITAL WARTS)
CONGENITAL ANOMALIES
CONGENITAL ANOMALY, UNSPECIFIED
CONGENITAL CATARACTS (UNSPECIFIED)
CONGENITAL CRANIOFACIAL ANOMALIES
CONGENITAL CYSTIC ADENOMATOID MALFORMATION
CONGENITAL DISLOCATION OF HIP, BILATERAL
CONGENITAL ECTODERMAL DYSPLASIAS
CONGENITAL ERYTHROPOIETIC PORPHYRIA
CONGENITAL FACE AND NECK ANOMALIES
CONGENITAL GENERALIZED FIBROMATOSIS (DESMOID TUMOR)
CONGENITAL HEART DEFECTS (UNSPECIFIED ANOMALY, CONGENITAL HEART DISEASE)
CONGENITAL HERPES SIMPLEX (NEONATAL)
CONGENITAL HIP DYSPLASIA
CONGENITAL NYSTAGMUS
CONGENITAL OCULOMOTOR APRAXIA (COGAN'S SYNDROME TYPE II)
CONGENITAL PTOSIS
CONGENITAL PULMONARY STENOSIS
CONGENITAL RUBELLA (CONGENITAL GERMAN MEASLES)
CONGENITAL SPONDYLOEPIPHYSEAL DYSPLASIA (SED CONGENITAL)
CONGENITAL SYPHILIS
CONGENITAL/NEONATAL HYDRONEPHROSIS
CONN SYNDROME (PRIMARY ALDOSTERONISM, PRIMARY HYPERALDOSTERONISM)
CONRADI-HUNERMANN SYNDROME
CONSTIPATION
CONTACT DERMATITIS (DERMATITIS MEDICAMENTOSA, DERMATITIS VENENATA)
COR TRIATRIATUM (TRIATRIAL HEART)
CORNEA TRANSPLANT
CORNEAL DYSTROPHY/STROMAL DYSTROPHY
CORNELIA DE LANGE SYNDROME (BRACHMANN-DE LANGE)
CORTICAL VISUAL IMPAIRMENT (CVI) / CORTICAL BLINDNESS
COSTELLO SYNDROME
COXSACKIE VIRUS (HAND-FOOT-MOUTH DISEASE, VESICULAR STOMATITIS)
CRANIOFACIAL DYSTOSIS (CROUZON DISEASE)
CRANIOPHARYNGIOMA (BRAIN TUMOR)
CREUTZFELDT-JAKOB DISEASE (SPASTIC PSEUDOSCLEROSIS, SPONGIOFORM ENCEPHALOPATHY)
CRI-DU-CHAT SYNDROME (5P SYNDROME, CAT'S CRY SYNDROME))
CROHN'S DISEASE
CROUP
CRYPTORCHISM
CUSHING'S SYNDROME
CUTANEOUS NECROTIZING VASCULITIS
CUTIS LAXA
CUTIS MARMORATA TELANGIECTATICA CONGENITA (CMTC)
CYCLIC NEUTROPENIA ( CN, PERIODIC NEUTROPENIA)
CYCLIC VOMITING SYNDROME (CVS)
CYSTIC FIBROSIS (CF)
CYSTIC HYGROMA (LYMPHANGIOMA)
CYSTIC LYMPHANGIOMA
CYSTINOSIS
CYTOMEGALOVIRUS (CMV)
DANDY-WALKER SYNDROME
DEAF - BLIND
DEAF / HARD OF HEARING
DEATH OF A YOUNG ADULT
DEATH OF CHILD (SEE ALSO INFANT DEATH)
DEJERINE-SOTTAS DISEASE
DEMENTIAS
DENTAL DISORDERS (UNSPECIFIED, TEETH)
DENTOFACIAL ANOMALIES - ORAL/FACIAL DISORDERS/DISFIGUREMENTS
DEPRESSION (MAJOR, NON-BIPOLAR, UNIPOLAR)
DERMATITIS ATOPIC (ATOPIC ECZEMA, BESNIER PRURIGO)
DERMATITIS HERPETIFORMIS
DERMATOMYOSITIS, JUVENILE (JDMS, CHILDHOOD DERMATOMYOSITIS)
DES (DIETHYLSTILBESTROL)
DEVELOPMENTAL APHASIA (CONGENITAL APHASIA, APHASIC)
DEVELOPMENTAL DELAY/DISABILITY
DEXTROCARDIA WITH SITUS INVERSUS (MIRROR-IMAGE DEXTROCARDIA))
DIABETES INSIPIDUS (DI)
DIAPHRAGMATIC HERNIA
DIARRHEA
DIGEORGE SYNDROME
DISCOID LUPUS ERYTHEMATOSUS (DLE, CHRONIC, CAZENAVE'S, NONDISSEMINATED)
DISORDER OF BONE AND CARTILAGE
DISORDER OF URETHRA OR URINARY TRACT (UNSPECIFIED)
DISSOCIATIVE IDENTITY DISORDER (DID, MULTIPLE PERSONALITY DISORDER, MPD)
DIVERTICULITIS
DO NOT USE--USE 282.0 SPHEROCYTIC HEMOLYTIC ANEMIA (MINKOWSKI-CHAUFFARD)
DOPA-RESPONSIVE DYSTONIA (HEREDITARY PROGRESSIVE, SEGAWA'S DYSTONIA)
DOWN SYNDROME (TRISOMY 21, TRISOMY G, TRANSLOCATION 21, MOSAICISM)
DOWN SYNDROME / AUTISTIC SPECTRUM DISORDER (DS-ASD)
DPT
DROWNED, DROWNING
DRUG ABUSE/ADDICTION
DRUG EXPOSURE DURING PREGNANCY (EFFECTS UPON INFANT)
DUAL DIAGNOSIS (MENTAL RETARDATION/MENTAL ILLNESS)
DUANE SYNDROME
DUBIN JOHNSON SYNDROME (DJS)
DUBOWITZ SYNDROME (INTRAUTERINE DWARFISM)
DUMPING SYNDROME
DYSCALCULIA (MATH LEARNING DISABILITY)
DYSCHROMIA, HYPOPIGMENTATION
DYSGENESIS OF THE CORPUS CALLOSUM
DYSGRAPHIA
DYSLEXIA (DEVELOPMENTAL)
DYSLEXIA (SECONDARY TO ORGANIC LESION)
DYSTHYMIA (DEPRESSIVE NEUROSIS, MILD DEPRESSION)
DYSTONIA (IDIOPATHIC TORSION DYSTONIA, ITD, GENERALIZED)
DYSTROPHIC EPIDERMOLYSIS BULLOSA
EAR DISORDERS
EATON LAMBERT SYNDROME
EBSTEINS ANOMALY
ECTOPIC PREGNANCY
ECTRODACTYLY ECTODERMAL DYSPLASIA CLEFT LIP/PALATE (EEC SYNDROME)
EHLERS-DANLOS SYNDROME
ELECTIVE MUTISM (SELECTIVE MUTISM)
ELLIS VAN CREVELD SYNDROME
EMPHYSEMA
EMPTY SELLA SYNDROME (EMPTY SELLA TURCICA)
ENCEPHALITIS (VIRAL)
ENCEPHALOCELE
ENDOMETRIOSIS
ENDOMYOCARDIAL FIBROSIS (DAVIES' DISEASE, LOEFFLER'S DISEASE, FIBROELASTIC ENDOC
ENGELMANN DISEASE (PROGRESSIVE DIAPHYSEAL DYSPLASIA)
EOSINOPHILIA MYALGIA SYNDROME (EMS)
EPENDYMOMA (BRAIN TUMOR)
EPIDERMAL NEVUS SYNDROME (LINEAR SEBACEOUS NEVUS SYNDROME)
EPIDERMOLYTIC HYPERKERATOSIS
EPILEPSY (SEIZURE DISORDERS)
EPILEPSY, MYOCLONIC PROGRESSIVE FAMILIAL
EPIPHYSEALIS HEMIMELICA DYSPLASIA (ACLASIS, TARSOEPIPHYSEAL)
ERB'S PALSY (A TYPE OF BRACHIAL PLEXUS INJURY, DUCHENNE PALSY)
ERYSIPELAS (SAINT ANTHONY FIRE)
ERYTHEMA INFECTIOSUM (FIFTH DISEASE)
ERYTHEMA MULTIFORME (STEVENS-JOHNSON SYNDROME)
ESOPHAGEAL ATRESIA, TRACHEOESOPHAGEAL FISTULA
EWING'S SARCOMA (EWING TUMOR, ENDOTHELIAL MYELOMA)
EXOTROPIA
EXSTROPHY OF BLADDER
EYE (OPHTHALMOLOGIC) DISORDERS
FABRY DISEASE
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY
FACTOR V (PARAHEMOPHILIA)
FAHR'S DISEASE
FAILURE TO THRIVE (FTT)
FAIRBANK DISEASE (MULTIPLE EPIPHYSEAL DYSPLASIA)
FAMILIAL ADENOMATOUS POLYPOSIS (FAP, GARDNER SYNDROME, POLYPOSIS OF THE COLON)
FAMILIAL DYSAUTONOMIA (RILEY-DAY SYNDROME, HEREDITARY SENSORY NEUROPATHY III)
FANCONI'S ANEMIA
FECAL INCONTINENCE (ENCOPRESIS)
FEEDING PROBLEMS
FEMORAL-FACIAL SYNDROME
FETAL ALCOHOL SYNDROME (FAS, FAE, ALCOHOL EXPOSURE DURING PREGNANCY)
FETAL AND NEONATAL JAUNDICE (UNSPECIFIED, HYPERBILIRUBINEMIA))
FETAL HYDANTOIN SYNDROME (FHS, DILANTIN EFFECTS)
FETAL VALPROATE SYNDROME (FETAL EFFECTS FROM EXPOSURE TO VALPROIC ACID)
FG SYNDROME
FIBER TYPE DISPROPORTION, CONGENITAL (MYOPATHY OF CONGENITAL FIBER TYPE DISPROPORTION)
FIBROMYOSITIS (FIBROMYALGIA, FIBROSITIS, MUSCULAR RHEUMATISM, TENSION MYALGIA)
FIBROUS DYSPLASIA (MONOSTOTIC, SOLITARY)
FLOATING HARBOR SYNDROME
FOCAL DERMAL HYPOPLASIA (COMBINED MESOECTODERMAL DYSPLASIA, MESODERMAL AND ECTOD
FOCAL DYSTONIA - FACIAL (BLEPHAROSPASM)
FOOD ALLERGY
FORBES DISEASE - AMYLO-1,6-GLUCOSIDASE DEFICIENCY - GLYCOGEN STORAGE DISEASE III
FRACTURE
FRAGILE X SYNDROME (FRAXA, MARTIN-BELL SYNDROME)
FRASER SYNDROME (CRYPTOPHTALMOS SYNDACTYLY SYNDROME)
FREEMAN-SHELDON SYNDROME (WHISTLING FACE SYNDROME, CRANIOCARPOTARSAL DYSTROPHY)
FRIEDREICH'S ATAXIA
FRONTONASAL DYSPLASIA SEQUENCE (MEDIAN CLEFT FACE SYNDROME)
FRUCTOSURIA
FRYNS SYNDROME
FUNCTIONAL DIGESTIVE DISORDER
FUNDUS ALBIPUNCTATUS
FUNDUS FLAVIMACULATUS
GALACTOSEMIA
GASTRO-INTESTINAL CANCER
GASTROENTERITIS (EOSINOPHILIC)
GASTROENTEROLOGIC/ GASTROPARESIS (STOMACH/ DIGESTIVE DISORDERS)
GASTROESOPHAGEAL REFLUX (GER)
GASTROSCHISIS
GAUCHER DISEASE (SEE ALSO GENETIC DISORDERS)
GENITAL HERPES (HERPES SIMPLEX VIRUS)
GEOGRAPHIC TONGUE (BENIGN MIGRATORY GLOSSITIS)
GERSTMANN SYNDROME
GIANOTTI-CROSTI SYNDROME (ACRODERMATITIS, PAPULAR)
GIANT CELL ARTERITIS (GCA, GRANULOMATOUS ARTERITIS)
GIANT CONGENITAL NEVUS (CONGENITAL NEVI, GIANT NEVUS))
GILBERT SYNDROME (FAMILIAL JAUNDICE, HYPERBILIRUBINEMIA 1)
GLAUCOMA (SEVERAL TYPES, SEE ALSO VISION IMPAIRED)
GLIOBLASTOMA MULTIFORME (MALIGNANT GLIOMA, BRAIN TUMOR)
GLUCOSE-GALACTOSE MALABSORBTION SYNDROME
GLUTARIC ACIDEMIA I (GA I, GLUTARIC ACIDURIA I)
GLUTARIC ACIDEMIA II ( GA II, GLUTARIC ACIDURIA II, MAD)
GOLDENHAR SYNDROME (OCULOAURICULOVERTEBRAL DYSPLASIA, OAV SYNDROME)
GOODPASTURE SYNDROME (PNEUMORENAL)
GORDON SYNDROME (DISTAL ARTHROGRYPOSIS)
GOTTRON'S SYNDROME (FAMILIAL ACROGERIA, FAMILIAL ACROMICRIA))
GRAFT VERSUS HOST DISEASE (GVHD)
GRAVES DISEASE (HYPERTHYROIDISM)
GROUP B STREP (SEPTICEMIA OF NEWBORN)
GROWTH HORMONE DEFICIENCY
GUILLAIN-BARRE SYNDROME (ACUTE IDIOPATHIC POLYNEURITIS, POSTINFECTIOUS POLYNEURITIS)
GULF WAR SYNDROME (UNSPECIFIED CAUSES)
HAEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS (HLH, FAMILIAL HLH, ERYTHROPHAGOCYTIC)
HAIRY CELL LEUKEMIA (LEUKEMIC RETICULOENDOTHELIOSIS)
HAJDU-CHENEY SYNDROME
HALLERMANN-STREIFF SYNDROME
HALLERVORDEN-SPATZ SYNDROME
HARTNUP DISEASE
HASHIMOTO THYROIDITIS (CHRONIC LYMPHOCYTIC THYROIDITIS)
HAY-WELL'S SYNDROME (ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE)
HEAD INJURY (TRAUMATIC BRAIN INJURY, TBI, INTRACRANIAL INJURY)
HEAD LICE
HEART (CARDIOLOGIC) DISORDERS
HEART MURMUR
HELLP SYNDROME (SEVERE PREECLAMPSIA)
HEMANGIOMA
HEMANGIOMA-THROMBOCYTOPENIA (KASABACH-MERRITT SYNDROME)
HEMIFACIAL MICROSOMIA
HEMIPLEGIA
HEMOCHROMATOSIS (SEE ALSO HEMATOLOGIC DISORDERS)
HEMOGLOBIN SC DISEASE (SICKLE C DISEASE)
HEMOLYTIC UREMIC SYNDROME
HEMOPHILIA (SEE ALSO HEMATOLOGIC DISORDERS)
HENOCH SCHONLEIN PURPURA
HEPATITIS A
HEPATITIS B (HBV)
HEPATITIS C
HEPATOBLASTOMA
HEREDITARY ANGIOEDEMA (ANGIONEUROTIC EDEMA, HAE, HANE, C1-INH))
HEREDITARY ATAXIA (CEREBELLAR DEGENERATION; FORMERLY MARIES ATAXIA)
HEREDITARY FRUCTOSE INTOLERANCE
HEREDITARY HEMORRHAGIC TELANGIECTASIA (HHT, OSLER WEBER RENDU SYNDROME)
HEREDITARY NONSPHEROCYTIC HEMOLYTIC ANEMIA (HNHA, NSA)
HEREDITARY SENSORY NEUROPATHY TYPE I (SENSORY RADICULAR NEUROPATHY, HSN-I)
HEREDITARY SENSORY NEUROPATHY TYPE II (CONGENITAL SENSORY NEUROPATHY, HSN-II)
HEREDITARY SPASTIC PARAPLEGIA (HSP, STRUMPELL-LORRAIN, FAMILIAL, FSP)
HEREDITARY SPHEROCYTIC HEMOLYTIC ANEMIA (ACHOLURIC JAUNDICE, SPHEROCYTOSIS)
HERMANSKY-PUDLAK SYNDROME
HERPES ZOSTER (SHINGLES, VARICELLA ZOSTER)
HERPETIC ENCEPHALITIS
HICCUPS
HIRSCHSPRUNG'S DISEASE (MEGACOLON)
HODGKIN'S DISEASE
HOLOPROSENCEPHALY (ARHINENCEPHALY, HS)
HOLT ORAM SYNDROME
HOMOCYSTINURIA (HOMOCYSTINEMIA)
HORNER SYNDROME (OCULOSYMPATHETIC PALSY, BERNARD-HORNER SYNDROME)
HUMAN IMMUNODEFICIENCY VIRUS (HIV INFECTION, SYMPTOMATIC)
HUMAN PAPILLOMAVIRUS (HPV)
HUNTER SYNDROME (MUCOPOLYSACCHARIDOSIS TYPE II, MPS II)
HUNTINGTON'S DISEASE (SEE ALSO NEUROLOGIC DISORDERS)
HURLER SYNDROME (MPS I)
HUTCHINSON-GILFORD SYNDROME (PROGERIA OF CHILDHOOD)
HYDRANENCEPHALY
HYDROCEPHALUS (CONGENITAL, SEE ALSO NEUROLOGIC DISORDERS)
HYPERCALCEMIA, HYPOCALCEMIA (HIGH/LOW CALCIUM BLOOD CONTENT)
HYPERCHOLESTEROLEMIA
HYPEREXPLEXIA (KOK DISEASE, STARTLE DISEASE)
HYPERHIDROSIS
HYPERKALEMIA (HYPERPOTASSEMIA)
HYPERLEXIA
HYPERTELORISM (SKULL AND FACE BONE ANOMALY)
HYPERTENSION (CHRONIC)
HYPERTENSION WITH PRE-ECLAMPSIA OR ECLAMPSIA
HYPOCHONDROPLASIA (ATYPICAL ACHONDROPLASIA)
HYPOGENESIS OF THE CORPUS CALLOSUM
HYPOGLYCEMIA
HYPOHIDROTIC ECTODERMAL DYSPLASIA
HYPOKALEMIA
HYPOMELANOSIS OF ITO
HYPOMYELINATION (DELAYED MYELIN, INSUFFICIENT MYELIN, INCOMPLETE MYELIN)
HYPOPHOSPHATASIA (HYPERCALCIURIC RICKETS, HHRH)
HYPOPHOSPHATEMIC RICKETS
HYPOPLASIA OF THE CORPUS CALLOSUM
HYPOPLASTIC LEFT HEART SYNDROME (HLHS) / AORTIC ATRESIA
HYPOSPADIAS / EPISPADIAS
HYPOTHYROIDISM
HYPOXIC ISCHEMIC ENCEPHALOPATHY (BRAIN INJURY)
HYPOXIC-ANOXIC BRAIN INJURY
ICHTHYOSIS (ALL TYPES)
ICHTHYOSIS CONGENITA (CONGENITAL ICHTHYOSIFORM ERYTHRODERMA, CIE)
IDIOPATHIC DIFFUSE INTERSTITIAL PULMONARY FIBROSIS
IDIOPATHIC EDEMA (CYCLIC, DISTRESS, PERIODIC, OR STRESS EDEMA)
IDIOPATHIC MYELOFIBROSIS (OSTEOSCLEROSIS, AGNOGENIC MYELOID METAPLASIA, AMM)
IDIOPATHIC THROMBOCYTOPENIC PURPURA (ITP)
IGA NEPHROPATHY (KIDNEY)
IMMUNE DEFICIENCY
IMMUNIZATION/VACCINATION - CHICKEN POX (VARICELLA)
IMMUNIZATION/VACCINATION - DIPHTHERIA, TETANUS-PERTUSSIS (DTP)
IMMUNIZATION/VACCINATION - HAEMOPHILUS INFLUENZAE TYPE B DISEASE (HIB)
IMMUNIZATION/VACCINATION - HEPATITIS B
IMMUNIZATION/VACCINATION - MEASLES, MUMPS, RUBELLA (MMR)
IMMUNIZATION/VACCINATION - POLIO (OPV, IPV)
IMMUNIZATION/VACCINATION - TETANUS AND DIPHTHERIA (TD)
IMMUNOLOGIC DISORDERS (UNSPECIFIED, NONSPECIFIC)
IMMUNOTHERAPY
IMPERFORATE ANUS (ANAL ATRESIA, ANAL STENOSIS, PERINEAL ANUS)
IMPETIGO
INCLUSION BODY MYOSITIS (IBM)
INCONTINENTIA PIGMENTI (BLOCH-SULZBERGER SYNDROME)
INFANT DEATH (AFTER DELIVERY, UNSPECIFIED CAUSE)
INFANTILE ANOREXIA (FEEDING DISTURBANCES, APPETITE LOSS IN INFANTS, NONORGANIC)
INFANTILE APNEA (REPIRATORY DISTRESS, CYANOTIC ATTACKS)
INFANTILE SPASM
INFECTIOUS DISEASES
INFERTILITY - FEMALE
INFERTILITY - MALE
INFLUENZA
INHALANT ABUSE (SOLVENT ABUSE, GLUE SNIFFING, VOLATILE SUBSTANCE ABUSE)
INHALENT EXPOSURE DURING PREGNANCY (FETAL INHALENT SYNDROME)
INIENCEPHALY
INJURY BY FIREARMS (GUNSHOT WOUNDS)
INTERMEDIATE SPINAL MUSCULAR ATROPHY, TYPE II (SMA II)
INTERMITTENT EXPLOSIVE DISORDER
INTERSEXUALITY (HERMAPHRODITISM, AMBIGUOUS SEXUALITY)
INTERSTITIAL 2Q- (2 Q MINUS)
INTERSTITIAL CYSTITIS
INTERSTITIAL PNEUMONIA (CHRONIC FIBROUS PNEUMONIA)
INTESTINAL DISORDER
INTESTINAL PSEUDO-OBSTRUCTION (CONGENITAL SHORT BOWEL, POST-SURGICAL SHORT BOWEL)
INTRAUTERINE GROWTH RETARDATION
INTRAVENTRICULAR HEMORRHAGE (IVH, PVH, PERIVENTRICULAR HEMORRHAGE))
IRON DEFICIENCY ANEMIA
IRRITABLE BOWEL SYNDROME (SPASTIC COLON, IBS)
ISODICENTRIC 15 (IDIC 15, INVERTED DUPLICATION 15,INV DUP [15])
IVEMARK SYNDROME (ASPLENIA SYNDROME, SPLENIC AGENESIS SYNDROME)
JACKSON WEISS SYNDROME
JAPANESE ENCEPHALITIS
JARCHO-LEVIN SYNDROME (SPONDYLOTHORACIC DYSPLASIA)
JEUNE SYNDROME (ASPHYXIATING THORACIC DYSTROPHY, ATD)
JOB SYNDROME (HYPER-IGE SYNDROME, HIE SYNDROME)
JOUBERT'S SYNDROME
JUMPING FRENCHMAN OF MAINE ( LATAH, MYRIACHIT)
JUVENILE CATARACTS
JUVENILE RHEUMATOID ARTHRITIS
KABUKI MAKE-UP SYNDROME (KMS, NIIKAWAKUROKI SYNDROME)
KALLMANN SYNDROME
KARTAGENER TRIAD (SINUSITIS, BRONCHIECTASIS, SITUS INVERSUS)
KAWASAKI DISEASE (MUCOCUTANEOUS LYMPH NODE SYNDROME)
KEARNS SAYRE SYNDROME (CPEO, CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA W/MYOPATHY)
KENNEDY DISEASE (SPINAL AND BULBAR MUSCULAR ATROPHY, SBMA)
KERATOCONUS ( CONICAL CORNEA, CONGENITAL KERATOCONUS)
KERNICTERUS
KIDNEY CANCER
KIDNEY DISORDER / KIDNEY DISEASE
KIDNEY DISORDERS (MALROTATION,FUSION,HORSESHOE,DUPLICATION,HYPERPLASIA, ETC)
KINSBOURNE SYDNROME (MYCLONIC ENCEPHALOPATHY)
KLINEFELTER SYNDROME (CHROMOSOME XXY OR 48 XXXY/XXYY, PRIMARY HYPOGONADISM)
KLIPPEL-FEIL SYNDROME
KLIPPEL-TRENAUNAY-WEBER SYNDROME (ANGIO-OSTEOHYPERTROPHY)
KRABBE'S LEUKODYSTROPHY (GALACTOCEREBROSIDASE DEFICIENCY, SPHINOGOLIPIDOSIS, GLOBOID)
KUGELBERG-WELANDER SYNDROME (JUVENILE SPINAL MUSCULAR ATROPHY TYPE III, SMA III)
KYPHOSIS
LACTOSE INTOLERANCE (ALACTASIA)
LADD'S SYNDROME (DUODENAL STENOSIS)
LAMELLAR RECESSIVE ICHTHYOSIS
LANDAU-KLEFFNER SYNDROME
LANGERHANS CELL HISTIOCYTOSIS (LCH, HISTIOCYTOSIS-X, HAND-SCHULLER-CHRISTIAN)
LARON DWARFISM (PITUITARY DWARFISM)
LARSEN SYNDROME
LARYNGOMALACIA
LATEX ALLERGY
LAURENCE-MOON SYNDROME (ADIPOGENITAL-RENTINITIS PIGMENTOSA , LM SYNDROME)
LEAD POISONING (TOXIC EFFECTS OF ALL LEAD COMPOUNDS)
LEARNING DISABILITIES (LD) (SEE ALSO DEV. DELAY/DISABILITY)
LEBER HEREDITARY OPTIC NEUROPATHY (LHON)
LEBER'S CONGENITAL AMAUROSIS
LEGG-CALVE-PERTHES SYNDROME
LEIGH'S DISEASE
LEINER DISEASE
LENNOX-GASTAUT SYNDROME (LGS, ASTATIC PETIT MAL, DOOSE'S, HHE)
LENZ MICROPHTHALMIA SYNDROME
LEPRECHAUNISM (DONOHUE SYNDROME)
LEPROSY (HANSEN'S DISEASE)
LESCH-NYHAN SYNDROME
LEUKEMIA (SEE ALSO CANCER)
LEUKODYSTROPHY (SEE ALSO SPECIFIC TYPES OF LEUKODYSTROPHIES)
LICHEN SCLEROSUS (ET ATROPHICUS)
LIGNEOUS CONJUNCTIVITIS
LIMB-GIRDLE MUSCULAR DYSTROPHY (ERB MD, LGMD, PROXIMAL MD)
LIPOMYELOMENINGOCELE
LISSENCEPHALY (AGYRIA, MILLER-DIEKER SYNDROME)
LIVER DISORDERS (UNSPECIFIED, HEPATIC)
LOBAR EMPHYSEMA (CONGENITAL)
LOCKED-IN SYNDROME (CEREBROMEDULLOSPINAL DISCONNECTION; DE-EFFERENTED STATE; PSEUDOCOMA
LONG-CHAIN ACYL COA DEHYDROGENASE DEFICIENCY (LCAD DEFICIENCY)
LORDOSIS
LOSS OF LIMB-CONGENITAL (LOWER)
LOSS OF LIMB-CONGENITAL (UPPER)
LOWE SYNDROME (-TERREY-MACLACHLAN, OCULOCEREBRORENAL DYSTROPHY)
LUNG DISORDERS (UNSPECIFIED, PULMONARY)
LUPUS VULGARIS (MILITARIS DISSEMINATUS FACIEI, TUBERCULOSIS)
LYME DISEASE
LYMPHANGIOMA,CAVERNOUS
LYMPHANGIOMYOMATOSIS
LYMPHEDEMA, AQUIRED, SECONDARY
LYMPHEDEMA, HEREDITARY, CONGENITAL
LYMPHOCYTIC INFILTRATE OF JESSNER
LYMPHOMA (NON-HODGKINS, OTHER TYPES, NONSPECIFIED)
MACROGYRIA (PACHYGYRIA)
MACULAR DEGENERATION / STARGARDT'S DISEASE
MALARIA (AGUE, PALUDISM, JUNGLE FEVER, SWAMP FEVER)
MALIGNANT HYPERTHERMIA (DUE TO ANESTHESIA)
MALROTATION OF COLON (MALROTATION OF INTESTINE)
MANNOSIDOSIS (LYSOSOMAL ALPHA-D-MANNOSIDASE DEFICIENCY)
MAPLE SYRUP (URINE) DISEASE (MENKE'S)
MARCUS GUNN PHENOMENON/PTOSIS (JAW-WINKING OR MAXILLOPALPEBRAL SYNKINESIS)
MARDEN WALKER SYNDROME (MWS, CONNECTIVE TISSUE DISORDER MARDEN WALKER TYPE)
MARFAN SYNDROME (SEE ALSO GENETIC DISORDERS)
MARSHALL SYNDROME
MARSHALL-SMITH SYNDROME
MCCUNE ALBRIGHT SYNDROME
MECKEL SYNDROME (GRUBER SYNDROME, MECKEL-GRUBER SYNDROME)
MECONIUM ASPIRATION SYNDROME
MEDICALLY FRAGILE (SEE YF-300.495)
MEDIUM-CHAIN ACYL COA DEHYDROGENASE DEFICIENCY (MCAD DEFICIENCY)
MEDULLOBLASTOMA (BRAIN TUMOR)
MEGALENCEPHALY
MELANOMA
MELAS SYNDROME (MITOCHONDRIAL ENCEPHALOMYOPATHIES)
MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS (MPGN TYPE II)
MENIERE DISEASE
MENINGITIS (ADULT, INFANTILE, NEONATAL)
MENINGOCELE
MENINGOCOCCEMIA (MEMINGOCOCCAL DISEASE, MENINGOCOCCEMIA-MENINGITIS)
MENKES' SYNDROME
MENTAL ILLNESS/BEHAVIORALLY/EMOTIONALLY DISTURBED (BEH)
MENTAL RETARDATION (UNSPECIFIED)
MERRF SYNDROME (MITOCHONDRIAL ENCEPHALOMYOPATHIES, FUKUHARA SYNDROME)
METABOLIC AND MITOCHONDRIAL DISORDERS (CARNITINE DEFICIENCY SYNDROMES)
METACHROMATIC LEUKODYSTROPHY (MLD, LEUKOENCEPHALOPATHY, DIFFUSE CEREBRAL SCLEROSIS, SULFATIDOSIS)
METAPHYSEAL CHONDRODYSPLASIA, MCKUSICK TYPE (CARTILAGE-HAIR HYPOPLASIA, CHH)
METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE (SCHMID METAPHYSEAL DYSTOSIS)
METATROPIC DYSPLASIA/HYPERPLASTIC CHONDRODYSTROPHY/METATROPIC DWARFISM
METHEMOGLOBINEMIA
METHYLMALONIC ACIDEMIAS (METHYLMALONIC ACIDURIAS)
MICROCEPHALUS (MICROCEPHALY, MICROENCEPHALY, HYDROMICROCEPHALY)
MICROTIA
MICROVILLUS INCLUSION DISEASE (DAVIDSON'S DISEASE, FAMILIAL ENTEROPATHY)
MIGRAINE HEADACHE (VASCULAR HEADACHE)
MILD MENTAL RETARDATION (EMH)
MILLER SYNDROME (POSTAXIAL ACROFACIAL DYSOSTOSIS)
MISCARRIAGE (SEE ALSO STILLBIRTH)
MISSING CHILDREN/RUNAWAYS
MITRAL VALVE PROLAPSE SYNDROME
MIXED CONNECTIVE TISSUE DISEASE (MCTD)
MOBIUS SYNDROME (MOEBIUS SYNDROME)
MODERATE MENTAL RETARDATION (TMH)
MONOSOMY 9P (9P- SYNDROME, 9 P MINUS, RING 9, 9P2, ALFI'S SYNDROME)
MORBID OBESITY
MORQUIO SYNDROME (MUCOPOLYSACCHARIDOSIS IV, MPS IV)
MORRIS SYNDROME (TESTICULAR FEMINIZATION,GOLDBERG-MAXWELL SYNDROME))
MOSAIC TRISOMY 16
MOTOR DELAY (MOTOR DEVELOPMENT DISORDER)
MOYAMOYA
MUCOPOLYSACCHARIDOSIS (MPS)
MULLERIAN APLASIA
MULTIFOCAL ATRIAL TACHYCARDIA
MULTIPLE BIRTHS (MATERNAL COMPLICATIONS)
MULTIPLE CARBOXYLASE DEFICIENCY (BIOTINIDASE DEFICIENCY, HOLOCARBOXYLASE)
MULTIPLE CHEMICAL SENSITIVITY (MCS)
MULTIPLE CONGENITAL DISABILITIES (SEE ALSO DEVELOPMENTAL DELAY/DISABILITY))
MULTIPLE ENDOCRINE NEOPLASIA SYNDROMES (MEN)
MULTIPLE EXOSTOSES (DIAPHYSEAL ACLASIS)
MULTIPLE MYELOMA (SEE ALSO CANCER)
MULTIPLE PTERYGIUM SYNDROME (ESCOBAR SYNDROME)
MULTIPLE SCLEROSIS (MS) (SEE ALSO NEUROLOGIC DISORDERS)
MUNCHAUSEN SYNDROME
MUNCHAUSEN SYNDROME BY PROXY (FACTITIOUS ILLNESS BY PROXY)
MURDER
MUSCULAR DYSTROPHY (MD) (SEE ALSO NEUROLOGIC, GENETIC DISORDERS)
MYASTHENIA GRAVIS
MYASTHENIA GRAVIS (NEONATAL)
MYELITIS (MYELOPATHY)
MYELODYSPLASIA
MYELOMENINGOCELE
MYELOPROLIFERATIVE DISEASE
MYOCLONUS (INCLUDES PARAMYOCLONUS MULTIPLE, RAMSAY HUNT SYNDROME, OPSOCLONUS)
MYOSITIS OSSIFICANS (FIBRODYSPLASIA OSSIFICANS PROGESSIVA, FOP)
MYOTONIC DYSTROPHY (STEINERT DISEASE, MYOTONIA ATROPHICA, MYOTONIC DISORDERS)
MYOTUBULAR MYOPATHY (CENTRONUCLEAR MYOPATHY)
NAGER-DE REYNIER (DYSOSTOSIS MANDIBULARIS)
NAIL-PATELLA SYNDROME (FONG DISEASE, TURNER-KIESER SYNDROME)
NARCOLEPSY (GELINEAU'S SYNDROME, PAROXYSMAL SLEEP)
NECROTIZING ENTEROCOLITIS (NEC, ISCHEMIC, NEONATAL INFLAMMATORY BOWEL DISEASE)
NECROTIZING FASCIITIS
NEMALINE MYOPATHY (ROD MYOPATHY, CONGENITAL ROD DISEASE)
NEONATAL HEPATITIS (GIANT CELL HEPATITS, IDIOPATHIC NEONATAL HEPATITIS)
NEONATAL LUPUS
NEONATAL SEIZURES (NEWBORN SEIZURES)
NEPHROSIS (NEPHROTIC SYNDROME, SEE ALSO KIDNEY DISORDERS)
NEUROACANTHOCYTOSIS (ACANTHOCYTOSIS-NEUROLOGIC DISORDER, AMYOTROPIC CHOREA)
NEUROBLASTOMA (CHILDHOOD CANCER)
NEUROFIBROMATOSIS (SEE ALSO NEUROLOGIC, GENETIC DISORDERS)
NEUROLOGIC (NERVE) DISORDERS
NEUROMUSCULAR DISORDERS (UNSPECIFIED)
NEZELOFF SYNDROME
NIEMANN-PICK DISEASE
NIGHT TERRORS (PAVOR NOCTURNUS)
NON-KETOTIC HYPERGLYCINEMIA
NONVERBAL LEARNING DISABILITIES (RIGHT-HEMISPHERE LD, NLD, NVLD))
NOONAN SYNDROME (MALE TURNER SYNDROME, TURNER-ULLRICH, FEMALE PSEUDO-TURNER)
NORRIE (ANDERSON-WARBURG) SYNDROME
NOSE AND THROAT DISORDERS
NOT APPLICABLE
NOT DISABILITY RELATED
OBESITY (OVERWEIGHT)
OBSESSIVE COMPULSIVE DISORDER (OCD)
OCCULT SPINAL DYSRAPHISM (OSD, TETHERED CORD SYNDROME)
OCULO-GASTROINTESTINAL MUSCULAR DYSTROPHY
OLIVOPONTOCEREBELLAR ATROPHY (SPINOCEREBELLAR ATAXIA TYPES IV-VII; SCA TYPES 4-7
OLLIER DISEASE (OLLIER'S SYNDROME, CHONDRODYSPLASIA)
OMPHALOCELE
OPITZ SYNDROME (BBB, BBG, G SYNDROME, HYPERTELORISM-HYPOSPADIAS)
OPPOSITIONAL DEFIANT DISORDER (ODD)
OPTIC NERVE ATROPHY (ONA)
OPTIC NERVE DISEASE
OPTIC NERVE HYPOPLASIA
ORAL FACIAL DIGITAL SYNDROME (MOHR SYNDROME, OFD SYNDROME)
ORBITAL HYPERTELORISM
ORGAN TRANSPLANT
ORGANIC PERSONALITY SYNDROME
ORNITHINE TRANSCARBAMYLASE DEFICIENCY (HYPERAMMONEMIA II, UREA CYCLE DIS OTC)
ORTHOPEDIC DISORDERS
OSGOOD-SCHLATTER'S DISEASE (OSTEOCHONDROSIS, TIBIAL TUBERCLE)
OSTEOARTHRITIS
OSTEOGENESIS IMPERFECTA (BRITTLE BONE DISEASE; SEE ALSO GENETIC DISORDERS)
OSTEOMYELITIS
OSTEONECROSIS
OSTEOPETROSIS
OTAHARA SYNDROME (EARLY INFANTILE EPILEPTIC ENCEPHALOPATHY
OTHER AND UNSPECIFIED DISORDERS OF EATING
OTHER AND UNSPECIFIED DISORDERS OF METABOLISM
OTHER SEBORRHEIC DERMATITIS
OTITIS MEDIA (EAR INFECTION)
PACHYDERMOPERIOSTOSIS (HYPERTROPHIC OSTEOARTHROPATHY, TOURAINE-SOLENTE-GOLE)
PAGET'S DISEASE
PALLISTER-HALL SYNDROME
PALLISTER-KILLIAN MOSAIC SYNDROME (TESCHLER-NICOLA/KILLIAN, TETRASOMY 12P)
PALLISTER-W SYNDROME (W SYNDROME)
PANHYPOPITUITARISM (SHEEHAN'S SYNDROME, SIMMONDS DISEASE)
PANIC-ANXIETY SYNDROME (PANIC DISORDER)
PARALYSIS OF THE VOCAL CORDS (VOCAL FOLD PARALYSIS)
PARALYSIS, UNSPECIFIED
PARKINSON'S DISEASE (SEE ALSO NEUROLOGIC DISORDERS)
PAROXYSMAL DYSTONIAS (PAROXYSMAL DYSKINESIAS)
PAROXYSMAL SUPRAVENTRICULAR TACHYCARDIA (PSVT)
PARRY-ROMBERG SYNDROME
PARTIAL TRISOMY 1Q
PARTIAL TRISOMY 6Q
PATENT DUCTUS ARTERIOSUS (PDA)
PEDIATRIC NEUROTRANSMITTER DISEASE (TH DEFICIENCY, ALADD/AADC, DOPA-RESPONSIVE DYSTONIA, DHPR, SSADH)
PELIZAEUS-MERZBACHER BRAIN SCLEROSIS (DIFFUSE FAMILIAL BRAIN SCLEROSIS, SUDANOPHILIC LEUKODYSTROPHY)
PENDRED'S SYNDROME (FAMILIAL GOITER WITH DEAF-MUTISM)
PENTA X SYNDROME (49, XXXXX)
PENTALOGY OF CANTRELL (CANTRELL-HALLER-RAVICH SYNDROME)
PERIPHERAL NEUROPATHY (NEURITIS, MONONEUROPATHY, POLYNEUROPATHY)
PERIVENTRICULAR LEUKOMALACIA (PVL)
PERNICIOUS ANEMIA (ADDISON'S ANEMIA, PRIMARY ANEMIA)
PERSISTENT TRUNCUS ARTERIOSUS (BUCHANAN'S SYNDROME)
PERSISTENT VEGETATIVE STATE
PERTUSSIS (WHOOPING COUGH)
PERVASIVE DEVELOPMENTAL DISORDER (PDD)
PETER'S ANOMALY
PFEIFFER SYNDROME (ACROCEPHALOSYNDACTYLY V, ACS, NOACK)
PHENYLKETONURIA (PKU)
PHOBIAS
PHOCOMELIA SYNDROME
PICA (EATING DISORDER)
PICK'S DISEASE (LOBAR ATROPHY, DIFFUSE DEGENERATIVE CEREBRAL DISEASE)
PIERRE-ROBIN SYNDROME
PINEAL GLAND TUMOR (PINEAL REGION, BRAIN TUMOR)
PITUITARY GLAND AND HYPOTHALMUS DISORDERS (UNSPECIFIED)
PLASTIC/HAND/RECONSTRUCTIVE SURGERY
PNEUMOCYSTIS CARINII PNEUMONIA (PCP)
PNEUMOTHORAX
POEMS SYNDROME
POISONING
POISONING BY INSECTICIDE, PESTICIDE, OR HERBICIDE (UNSPECIFIED)
POLAND SYNDROME (POLAND SYNDACTYLY)
POLIO
POLYCYSTIC KIDNEY DISEASE (PKD)
POLYMYALGIA RHEUMATICA (ANARTHRITIC SYNDROME)
POLYMYOSITIS
POLYOSTOTIC FIBROUS DYSPLASIA OF BONE
POLYPHAGIA (EXCESSIVE EATING)
PORENCEPHALIC CYST/PORENCEPHALY (ACQUIRED)
PORENCEPHALIC CYST/PORENCEPHALY (CONGENITAL)
PORPHYRIA
PORT-WINE STAIN
POST-POLIO SYNDROME
POST-TRAUMATIC STRESS DISORDER/PTSD (CHRONIC, PROLONGED)
POSTERIOR UVEITIS (CHOROIDITIS)
POTT'S DISEASE (SPINAL CURVATURE, TUBERCULOSIS OF THE SPINE)
POVERTY
PRADER-WILLI SYNDROME (HYPOTONIA-HYPOMENTIA-HYPOGONADISM-OBESITY, HHHO)
PRECOCIOUS PUBERTY (PUBERTAS PRAECOX, FAMILIAL TESTOXICOSIS)
PREGNANCY
PREGNANCY TERMINATION (LEGAL ABORTION)
PREMATURE BIRTH/LOW BIRTH WEIGHT/PREMATURITY (SEE ALSO RISK)
PRIMARY BILIARY CIRRHOSIS (HANOT'S CIRRHOSIS, PBC)
PRIMARY CRANIOSYNOSTOSIS (CRANIOSTENOSIS, CSO, KLEEBLATTSCHADEL, PLAGIOCEPHALY)
PRIMARY PROGRESSIVE APHASIA
PRIMARY PULMONARY HYPERTENSION (PPH)
PRIMARY VISUAL AGNOSIA (VISUAL AMNESIA)
PROGRESSIVE OSSEOUS HETEROPLASIA (POH)
PROGRESSIVE SUPRANUCLEAR PALSY (PSP)
PROSTATE (GLAND, PRIMARY) CANCER
PROSTATE DISEASE
PROSTATITIS (CONGESTIVE,SUPPURATIVE)
PROTEUS SYNDROME
PROXIMAL FEMORAL FOCAL DEFICIENCY (PFFD)
PRUNE BELLY SYNDROME/EAGLE BARRETT SYNDROME
PSEUDO-HURLER POLYDYSTROPHY (MUCOLIPIDOSIS III, PSEUDOPOLYDYSTROPHY, GANGLIOSIDO
PSEUDOHYPOPARATHYROIDISM (MARTIN-ALBRIGHT SYNDROME, SEABRIGHT-BANTAM SYNDROME)
PSEUDOTUMOR CEREBRI (BENIGN OR IDIOPATHIC INTRACRANIAL HYPERTENSION
PSEUDOXANTHOMA ELASTICUM (PXE)
PSORIASIS
PSORIATIC ARTHRITIS (ARTHROPATHIC PSORIASIS)
PSYCHIATRIC DISORDERS
PULMONARY ALVEOLAR PROTEINOSIS (PHOSPHOLIPIDOSIS)
PULMONARY ATRESIA
PYKNODYSOSTOSIS (PYCNODYSOSTOSIS)
PYRUVATE DEHYDROGENASE DEFICIENCY (PDH DEFICIENCY, LACTIC & PYRIVATE ACIDEMIA)
PYRUVATE KINASE DEFICIENCY
RABIES (HYDROPHOBIA, LYSSA)
RAPE
RAPP-HODGKINS SYNDROME (DOMINANT HYPOHIDROTIC ECTODERMAL DYSPLASIA)
RASMUSSEN'S ENCEPHALITIS
RAYNAUD'S DISEASE & PHENOMENON
REACTIVE ATTACHMENT DISORDER (RAD)
RECURRENT RESPIRATORY PAPILLOMATOSIS (RRP, LARYNGEAL PAPILLOMA))
REDUCTION DEFORMITIES OF THE BRAIN
REFLEX SYMPATHETIC DYSTROPHY SYNDROME (RSDS) (COMPLEX REGIONAL PAIN SYNDROME) (CRPS)
REFSUM SYNDROME
REIFENSTEIN'S SYNDROME (PAIS, HEREDITARY FAMILIAL HYPOGONADIAM, MALE)
REITER'S SYNDROME (REITER'S DISEASE)
RENAL FAILURE (UNSPECIFIED, KIDNEY DISEASE)
RENAL TUBULAR ACIDOSIS (KIDNEY TUBULAR)
RESPIRATORY DISTRESS SYNDROME (RDS, HYALINE MEMBRANE DISEASE)
RESTLESS LEGS SYNDROME (EKBOM SYNDROME, ANXIETAS TIBIALIS, ACROMELALGIA)
RETINAL DEGENERATIVE DISEASES (DEGENERATIONS)
RETINITIS PIGMENTOSA (RP)
RETINOBLASTOMA
RETINOPATHY OF PREMATURITY (ROP, RLF, RETROLENTAL FIBROPLASIA)
RETINOSCHISIS
RETT SYNDROME
REYE SYNDROME
RH DISEASE (HYDROPS FETALIS, RH INCOMPATIBILITY, SEE ALSO HEMATOLOGIC DISORDERS
RHABDOMYOSARCOMA
RHEUMATIC CHOREA (SYDENHAM'S, ST. VITUS DANCE)
RHEUMATIC FEVER (WITHOUT HEART INVOLVEMENT, RHEUMATIC ARTHRITIS)
RHEUMATOLOGIC DISORDERS
RIEGER SYNDROME
RING 10 CHROMOSOME DISORDER (CHROMOSOME DELETION DISORDER)
RING 14 CHROMOSOME DISORDER
RING 15 CHROMOSOME DISORDER
RING 21 CHROMOSOME DISORDER
RING 6 CHROMOSOME DISORDER
RING 9 CHROMOSOME DISORDER
RISK (AT OR HIGH)
ROBERTS SYNDROME (HYPOMELIA-HYPOTRICHOSIS-FACIAL HEMANGIOMA, PSEUDOTHALIDOMIDE))
ROBINOW SYNDROME (FETAL FACE SYNDROME, ROBINOW DWARFING SYNDROME))
ROCKY MOUNTAIN SPOTTED FEVER
ROMANO WARD SYNDROME (QT PROLONGATION W/O CONGENITAL DEAFNESS)
ROSEOLA INFANTUM (EXANTHEM SUBITUM)
RUBELLA (GERMAN MEASLES, THREE-DAY MEASLES)
RUBINSTEIN-TAYBI SYNDROME (BROAD THUMB HALLUX SYNDROME)
RUSSELL-SILVER SYNDROME
SACRAL AGENESIS
SAETHRE-CHOTZEN SYNDROME (ACROCEPHALOSYNDACTYLY TYPE III)
SAKATI SYNDROME (ACROCEPHALOPOLYSYNDACTYLY TYPE III, ACPS III, W/ LEG HYPOPLASIA
SALICYLATE SENSITIVITY
SANDHOFF DISEASE (GANGLIOSIDOSIS GM2 TYPE 2)
SANDIFER'S SYNDROME
SANFILIPPO SYNDROME (MPS III)
SARCOIDOSIS
SARCOMA
SCAPULOPERONEAL MUSCULAR DYSTROPHY (SPD)
SCARLET FEVER
SCHINZEL ACROCALLOSAL SYNDROME (ACS, HALLUX DUPLICATION, POSTAXIAL POLYDACTYLY,
SCHIZENCEPHALY
SCHIZOPHRENIA
SCLERODERMA
SCOLIOSIS
SEASONAL AFFECTIVE DISORDER (SAD)
SEBORRHEA CAPITIS
SEBORRHEIC INFANTILE DERMATITIS
SEBORRHEIC KERATOSIS (ACANTHOTIC NEVUS, SEBORRHEIC WARTS)
SECKEL SYNDROME (NANOCEPHALY, MICROCEPHALIC PRIMORDIAL, BIRD-HEADED DWARFISM)
SECONDARY PULMONARY HYPERTENSION (SECONDARY PULMONARY ARTERIAL HYPERTENSION)
SEITELBERGER DISEASE (INFANTILE NEUROAXONAL DYSTROPHY)
SEIZURES (CONVULSIONS)
SELECTIVE IGA DEFICIENCY
SELF-STIMULATING BEHAVIORS (HEAD-BANGING, ROCKING, SELF-INJURIOUS BEHAVIORS))
SENSORY DISTURBANCE (TACTILE DEFENSIVENESS)
SENSORY INTEGRATIVE DISORDERS (SENSORY INTEGRATION DYSFUNCTION, SENSORY DEFENSIV
SEPTO-OPTIC DYSPLASIA (DE MORSIER DISEASE, DWARFISM-SEPTO-OPTIC DYSPLASIA)
SERPIGINOUS CHOROIDITIS
SEVERE COMBINED IMMUNODEFICIENCY ( SCID, ADENOSINE DEAMINASE DEFICIENCY, ADA)
SEVERE/PROFOUND MENTAL RETARDATION
SEX CHROMOSOME ANEUPLOIDY
SEX CHROMOSOME ANOMALIES (UNSPECIFIED)
SEXUAL ABUSE
SHAKEN BABY SYNDROME
SHORT CHAIN ACYL COA DEHYDROGENASE DEFICIENCY (SCAD)
SHORT STATURE
SHORT SYNDROME (REIGER ANOMALY-GROWTH RETARDATION)
SHPRINTZEN SYNDROME (VELOCARDIOFACIAL, VCF, DELETION OF 22Q11)
SHWACHMAN SYNDROME (- DIAMOND, - BODIAN)
SHY-DRAGER SYNDROME (PROGRESSIVE AUTONOMIC FAILURE, ORTHOSTATIC HYPOTENSION)
SIALIDOSIS (ALPHA-NEURAMINIDASE DEFICIENCY, MUCOLIPIDOSIS I)
SIALORRHEA (DROOLING, EXCESS SALIVATION)
SICK SINUS SYNDROME (BRADYCARDIA-TACHYCARDIA SYDROME)
SICKLE CELL BETA THALASSEMIA MINOR
SICKLE CELL DISEASE (SEE ALSO HEMATOLOGIC DISORDERS)
SIDEROBLASTIC ANEMIA (IRON OVERLOAD ANEMIA, SIDEROBLASTOSIS)
SIMPSON DYSMORPHIA SYNDROME (SIMPSON-GOLABI-BEHMEL, SGB, SDYS, BULLDOG SYNDROME)
SINGLE VENTRICLE (COMMON VENTRICLE)
SJOGREN'S SYNDROME (KERATOCONJUNCTIVITIS SICCA-KCS)
SKIN (DERMATOLOGIC) DISORDERS
SLEEP APNEA
SLEEP DISORDERS
SLY SYNDROME (MUCOPOLYSACCHARIDOSIS TYPE VII, BETA-GLUCURONIDASE DEFICIENCY)
SMALL FOR GESTATIONAL AGE (SGA)
SMITH-LEMLI-OPITZ SYNDROME
SMITH-MAGENIS SYNDROME (CHROMOSOME 17, INTERSTITIAL DELETION 17P)
SOCIAL ANXIETY DISORDER (SOCIAL PHOBIA)
SOTOS SYNDROME (CEREBRAL GIGANTISM)
SPASMODIC TORTICOLLIS (WRYNECK, CERVICAL DYSTONIA)
SPEECH AND LANGUAGE DISORDERS/DELAY
SPINA BIFIDA
SPINAL CORD INJURY (PARALYSIS, PARAPLEGIA, QUADRIPLEGIA, HEMIMYELIA)
SPINAL STENOSIS (LUMBAR, LUMBOSACRAL SPINAL STENOSIS)
SPLIT-HAND DEFORMITY (ECTRODACTYLY, LOBSTER CLAW DEFORMITY)
SPORTS MEDICINE
SPRENGEL DEFORMITY (CONGENITAL ELEVATION OF SCAPULA)
STICKLER SYNDROME (ARTHRO-OPHTHALMOPATHY)
STILLBIRTH (DEATH OF FETUS, PRE-DELIVERY DEATH)
STRABISMUS (UNSPECIFIED)
STRAWBERRY NEVUS
STREPTOCOCCAL SORE THROAT (STREP THROAT)
STRIDOR
STROKE (SEE ALSO NEUROLOGIC DISORDERS)
STURGE-WEBER SYNDROME (PARKES WEBER SYNDROME)
STUTTERING
SUBACUTE CEREBELLAR DEGENERATION
SUBARACHNOID HEMORRHAGE
SUBDURAL HYGROMA (LOCALIZED SUBDURAL HEMATOMA)
SUBGLOTTIC STENOSIS (NARROWING OF SUBGLOTTIC LARYNX)
SUDDEN INFANT DEATH SYNDROME (SIDS)
SUICIDE
SUMMITT SYNDROME (SUMMITT'S ACROCEPHALOSYNDACTYLY)
SWALLOWING DIFFICULTY (DYSPHAGIA)
SYNCOPE (FAINTING, BLACKOUT)
SYRINGOMYELIA
SYSTEMIC LUPUS ERYTHEMATOSUS (SLE, DISSEMINATED)
TARDIVE DYSKINESIA (TD, ORAL-FACIAL DYSKINESIA, LINGUOFACIAL DYSKINESIA)
TASTE DISORDERS / DISORDERS OF SMELL (ANOSMIA, PARAGEUSIA,PAROSMIA,AGEUSIA)
TAY-SACHS DISEASE (GM2 GANGLIOSIDOSIS TYPE I, HEXOSAMINIDASE ALPHA-SUBUNIT DEFICIENCY (VARIANT B))
TELECANTHUS (HYPERTELORISM-HYPOSPADIAS SYNDROME, DYSTOPIA CANTHORUM)
TEMPOROMANDIBULAR JOINT-PAIN-DYSFUNCTION SYNDROME (TMJ)
TENSION HEADACHE
TETRALOGY OF FALLOT
THALASSEMIA MAJOR (COOLEY'S ANEMIA, IRON OVERLOAD ANEMIA)
THROMBASTHENIA ( GLANZMANN DISEASE )
THROMBOCYTOPENIA
THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME (TAR SYNDROME)
THUMBSUCKING PROBLEM
THYROIDITIS
THYROTOXICOSIS
THYROTOXICOSIS
TIETZE SYNDROME (COSTOCHONDRITIS, COSTOCHONDRAL JUNCTION SYNDROME)
TORCH SYNDROME (TOXOPLASMOSIS-CYTOMEGALOVIRUS-HERPES SYNDROME)
TOURETTE SYNDROME (SEE ALSO NEUROLOGIC DISORDERS)
TOWNES SYNDROME (TOWNES BROCKS)
TOXIC EFFECT OF ASBESTOS
TOXOPLASMOSIS
TRACHEOMALACIA
TRACHEOSTOMY (TRACHEOTOMY) COMPLICATIONS
TRACHEOSTOMY / TRACHEOTOMY
TRACHEOSTOMY COMPLICATION (TRACHEOESOPHAGEAL FISTULA)
TRANSPOSITION OF THE GREAT VESSELS / TRANSPOSITION OF THE GREAT ARTERIES (TGA)
TRAUMA
TREACHER COLLINS SYNDROME (INCOMPLETE FACIAL DYSOSTOSIS)
TRICHORHINOPHALANGEAL SYNDROME TYPE I (TRP SYNDROME, TRPS1)
TRICHORHINOPHALANGEAL SYNDROME TYPE II (LANGER GIEDION SYNDROME, TRPS2)
TRICHORHINOPHALANGEAL SYNDROME TYPE III (TRPS3, SUGIO-KAJII SYNDROME)
TRICHORRHEXIS NODOSA
TRICHOTILLOMANIA (HAIR PULLING)
TRICUSPID ATRESIA
TRIGONOCEPHALY SYNDROME (C SYNDROME)
TRIMETHYLAMINURIA
TRIPLO X SYNDROME (TRIPLE X SYNDROME, 47,XXX SYNDROME))
TRIPLOIDY AND TRIPLOIDY MOSAICISM (69, XXX OR 69, XXY)
TRISMUS PSEUDOCAMPTODACTYLY SYNDROME (CAMPTODACTYLY-LIMITED JAW EXCURSION, HECHT
TRISOMY (UPSPECIFIED)
TRISOMY 12P
TRISOMY 13 (PATAU'S SYNDROME, TRISOMY 13-15, D TRISOMY)
TRISOMY 14 MOSAICISM SYNDROME
TRISOMY 18 (EDWARD'S SYNDROME, TRISOMY E, TRISOMY 16-18)
TRISOMY 19Q (DISTAL 19Q DUPLICATION)
TRISOMY 8P
TRISOMY 9 (CHROMOSOME 9P)
TRISOMY 9 MOSAIC (CHROMOSOME 9)
TUBERCULOSIS (UNSPECIFIED)
TUBEROUS SCLEROSIS (SEE ALSO NEUROLOGIC, GENETIC DISORDERS)
TURNER SYNDROME (GONADAL DYSGENESIS, OVARIAN DYSGENESIS, XO SYNDROME, MONOSOMY X
TWIN TO TWIN TRANSFUSION SYNDROME (TTTS)
TWINS/MULTIPLE BIRTH
TYPE 1 DIABETES (IDDM, INSULIN DEPENDENT DIABETES MELLITUS, JUVENILE DIABETES )
TYPE 2 DIABETES (ADULT-ONSET DIABETES, NONINSULIN-DEPENDENT DIABETES MELLITUS, NIDDM)
TYPHOID (TYPHOID FEVER, SALMONELLA TYPHI INFECTION)
TYROSINEMIA (TYROSYLURIA)
ULCERATIVE COLITIS
UNCODED DIAGNOSIS
UNKNOWN
UNSPECIFIED CARBOHYDRATE TRANSPORT AND METABOLISM DISORDERS
URINARY INCONTINENCE (ENURESIS)
URINARY TRACT INFECTION (UNSPECIFIED SITE)
USHER SYNDROME
UVEO-RETINAL COLOBOMA/COLOBOMATOUS MICROPHTHALMIA
VACCINE REACTION (COMPLICATIONS OF IMMUNIZATION/VACCINATION)
VACTERL SYNDROME ( VACTEL ASSOCIATION, VATER ASSOCIATION) )
VASCULITIS
VENEREAL DISEASE
VENTRICULAR SEPTAL DEFECTS (VSD)
VENTRICULAR TACHYCARDIA (WIDE-COMPLEX TACHYCARDIA)
VERTIGO/DIZZINESS
VESICOURETERAL REFLUX (URINARY REFLUX)
VIRAL RESPIRATORY INFECTION (RSV, RESPIRATORY SYNCTIAL VIRUS)
VISION IMPAIRED/BLIND/VISUALLY IMPAIRED
VISUAL PATHWAY AND HYPOTHALAMIC GLIOMA (OPTIC NERVE AND HYPOTHALAMUS, BRAIN TUMOR)
VITAMIN B 12 DEFICIENCY (COBALAMIN DEFICIENCY)
VITAMIN-D DEFICIENCY RICKETS
VITILIGO
VON GIERKE DISEASE (GLYCOGEN STORAGE DISEASE (G6PD DEFICIENCY)-GLUCOSE-6-PHOSPHATE DEHYDROGENASE)
VON HIPPEL-LINDAU DISEASE (ANGIOMATOSIS RETINA)
VON WILLEBRAND DISEASE
WAARDENBURG SYNDROME
WALDENSTROM MACROGLOBULINEMIA (HYPERGLOBULINEMIC PURPURA)
WALDMANN DISEASE (FAMILIAL DYSPROTEINEMIA; INTESTINAL LYMPHANGIECTASIA; IDIOPATHIC HYPOPROTEINEMIA
WALKER-WARBURG SYNDROME (CEREBROOCULAR DYSGENESIS, CHEMKE, PAGON, WARBURG, HARD)
WEAVER SYNDROME (WEAVER-SMITH SYNDROME)
WEGENER'S GRANULOMATOSIS SYNDROME
WELL CHILD
WERDNIG-HOFFMAN DISEASE (SPINAL MUSCULAR ATROPHY, TYPE I, SMA I)
WERNER SYNDROME (PROGERIA OF THE ADULT, PROGERIA ADULTORUM)
WEST SYNDROME
WIEDEMANN-RAUTENSTRAUCH SYNDROME (NEONATAL PROGEROID SYNDROME)
WILLIAMS SYNDROME
WILMS' TUMOR (SEE ALSO CANCER)
WILSON'S DISEASE
WISKOTT ALDRICH SYNDROME
WOLF-HIRSCHHORN SYNDROME (4P SYNDROME, CHROMOSOME NUMBER 4 SHORT ARM DELETION)
WOLFF-PARKINSON-WHITE SYNDROME
WOLFRAM SYNDROME
WYBURN-MASON SYNDROME (CEREBRORETINAL ARTERIOVENOUS ANEURYSM)
X-LINKED AGAMMAGLOBULINEMIA,CONGENITAL(BRUTON'S,CONGENITAL HYPOGAMMAGLOBULINEMIA
XERODERMA PIGMENTOSUM
XXXXY SYNDROME (49 XXXXY SYNDROME)
XYY SYNDROME (47,XYY KARYOTYPE)
YELLOW FEVER (BUNYAVIRUS INFECTION)
ZELLWEGER SYNDROME (CEREBROHEPATORENAL SYNDROME, BOWEN SYNDROME)