The Pediatric Database (PEDBASE) contains descriptions of over 550 childhood illnesses and has been on the Internet since November 15, 1995. Beginning in November of 1996, new diseases will be added and revisions made to existing files. Information on each disorder in this Database has been obtained from at least 3 sources including Nelson Textbook of Pediatrics (14th and 15th editions), the Birth Defects Encyclopedia (1990 and 1994 editions) and from at least one other source (journal articles, review articles, textbooks). One may download the entire Database as Shareware. An editable Registered version is also available through the author.

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• AARSKOG SYNDROME
• AASE SYNDROME
• ABETALIPOPROTEINEMIA
• ACATALASEMIA
• ACETAMINOPHEN OVERDOSE
• ACHONDROPLASIA
• ACID/ALKALI INGESTION
• ACNE VULGARIS
• ACUTE CEREBELLAR ATAXIA
• ACUTE INFECTIOUS LARYNGITIS
• ACUTE INTERMITTENT PORPHYRIA
• ACUTE SPASMODIC LARYNGITIS
• ACUTE TRACHEOBRONCHITIS
• ACUTE UVULITIS
• ADENOIDS
• ADENOVIRUS ENTERITIS
• ADRENOLEUKODYSTROPHY
• AEROMONAS ENTERITIS
• AGENESIS OF THE CORPUS CALLOSUM
• AGENESIS OF THE CEREBELLAR VERMIS
• AICARDI SYNDROME
• ALAGILLE SYNDROME
• ALEXANDER'S DISEASE
• ALLERGIC DISEASE
• ALPORT SYNDROME                                                                              
• ANEMIA - IRON DEFICIENCY
• ANEMIA - SIDEROBLASTIC
• ANEMIA OF CHRONIC DISEASE
• ANENCEPHALY
• ANGELMAN SYNDROME
• ANTERIOR UVEITIS
• APERT SYNDROME
• APLASTIC ANEMIA
• APLASTIC CRISIS
• ARGININEMIA
• ARGININOSUCCINIC ACIDURIA
• ASPHYXIATING THORACIC DYSTROPHY
• ASTHMA - ACUTE
• ASTHMA - ALLERGIC
• ASTHMA - CHRONIC
• ASTHMA - EXERCISE-INDUCED
• ASTROVIRUS ENTERITIS
• ATAXIA-TELANGIECTASIA
• ATAXIC DISORDERS
• ATOPIC DERMATITIS (ECZEMA)
• ATRANSFERRINEMIA
• ATRIAL SEPTAL DEFECT
• ATTENTION-DEFICIT HYPERACTIVITY DISORDER (ADHD)
• AUTOIMMUNE HEMOLYTIC ANEMIA-I
• AUTOIMMUNE HEMOLYTIC ANEMIA-II
• BACTERIAL MENINGITIS
• BACTERIAL TRACHEITIS
• BARAKAT'S SYNDROME
• BECKER DISEASE (MYOTONIA CONGENITA)
• BECKER MUSCULAR DYSTROPHY
• BECKWITH-WIEDEMANN SYNDROME                                                          
• BELL'S PALSY
• BENIGN CONGENITAL HYPOTONIA
• BENIGN FAMILIAL HEMATURIA
• BENIGN FAMILIAL NEONATAL SEIZURES
• BENIGN FRUCTOSURIA
• BENIGN HEREDITARY CHOREA
• BENIGN PAROXYSMAL VERTIGO
• BENIGN PARTIAL EPILEPSY WITH CENTROTEMPORAL SPIKES (BPEC)
• BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS
• BENIGN TRANSIENT PROTEINURIA
• BERNARD-SOULIER SYNDROME
• BLASTOCYSTIS HOMINIS ENTERITIS
• BLOCKED TEAR DUCT (DACRYOSTENOSIS)
• BLOOM SYNDROME
• BRAIN STEM GLIOMA
• BRONCHIOLITIS - ACUTE
• BRONCHIOLITIS OBLITERANS
• BRONCHOGENIC CYSTS
• BRUTON DISEASE
• BYLER DISEASE
• CAFFEY DISEASE
• CALICIVIRUS ENTERITIS
• CAMPYLOBACTER ENTEROCOLITIS
• CANAVAN'S DISEASE
• CARBAMOYL PHOSPHATE SYNTHETASE (CPS) DEFICIENCY
• CARTILAGE-HAIR HYPOPLASIA
• CAT SCRATCH DISEASE
• CELIAC DISEASE
• CENTRAL CORE DISEASE
• CENTRAL PONTINE MYELINOLYSIS
• CENTRONUCLEAR MYOPATHY
• CEREBELLAR ASTROCYTOMA
• CHARCOT-MARIE-TOOTH DISEASE
• CHEDIAK-HIGASHI SYNDROME
• CHILDHOOD ABSENCE EPILEPSY
• CHLAMYDIAL CONJUNCTIVITIS
• CHOLEDOCHAL CYST
• CHOLESTASIS - LYMPHEDEMA
• CHONDROECTODERMAL DYSPLASIA
• CHONDROMALACIA PATELLAE
• CHOREIC DISORDERS
• CHOTZEN SYNDROME
• CHRONIC BRONCHITIS                                                                                          
• CHRONIC COUGH
• CHRONIC GRANULOMATOUS DISEASE - X-LINKED
• CHRONIC MOTOR OR VOCAL TIC DISORDER
• CHRONIC MUCOCUTANEOUS CANDIDIASIS
• CHRONIC PERSISTENT DIARRHEA
• CITRULLINEMIA
• CLEIDOCRANIAL DYSOSTOSIS
• CLOSTRIDIUM PERFRINGENS ENTERITIS
• CNS TUMORS
• COARCTATION OF THE AORTA
• COCKAYNE SYNDROME
• COHEN SYNDROME
• COLIC
• COMMON VARIABLE IMMUNODEFICIENCY (CVID)
• COMPLEX PARTIAL SEIZURE (CPS)
• CONGENITAL PARVOVIRUS B19
• CONGENITAL BRONCHOBILIARY FISTULA
• CONGENITAL CMV
• CONGENITAL DYSERYTHROPOIETIC ANEMIA
• CONGENITAL HSV
• CONGENITAL HYPOTHYROIDISM
• CONGENITAL LOBAR EMPHYSEMA
• CONGENITAL MESOBLASTIC NEPRHOMA
• CONGENITAL MUSCLE FIBRE-TYPE DISPROPORTION
• CONGENITAL MUSCULAR DYSTROPHY
• CONGENITAL PULMONARY LYMPHANGECTASIA
• CONGENITAL RUBELLA
• CONGENITAL TOXOPLASMOSIS
• CONGENITAL VARICELLA
• CONSTIPATION
• CORNELIA DE LANGE SYNDROME
• COWDEN'S SYNDROME
• CRANIOSYNOSTOSIS
• CRI DU CHAT SYNDROME
• CRIGLER-NAJJAR SYNDROME - I
• CROHN'S DISEASE
• CROUP
• CROUZON SYNDROME
• CRYPTORCHIDISM
• CRYPTOSPORIDIUM ENTERITIS
• CYCLIC NEUTROPENIA
• CYCLIC VOMITING SYNDROME                                                                            
• CYSTIC ADENOMATOID MALFORMATION
• CYSTIC FIBROSIS
• CYSTIC HYGROMA
• CYSTINOSIS
• CYSTINURIA
• DANDY-WALKER MALFORMATION
• DEJERINE-SOTTAS DISEASE
• DEVELOPMENTAL DYSPLASIA OF THE HIP
• DIABETIC KETOACIDOSIS (DKA)
• DIAMOND-BLACKFAN SYNDROME
• DIARRHEA - ACUTE
• DIENCEPHALIC SYNDROME
• DIENTOMEBA FRAGILIS ENTERITIS
• DIETARY PROTEIN INTOLERANCE
• DIGEORGE ANOMALY
• DISTAL RENAL TUBULAR ACIDOSIS
• DOPA-RESPONSIVE DYSTONIA
• DOWN SYNDROME
• DUBIN-JOHNSON SYNDROME
• DUBOWITZ SYNDROME
• DYGGVE-MELCHIOR-CLAUSEN SYNDROME
• DYSKERATOSIS CONGENITA SYNDROME
• DYSTONIC DISORDERS
• ECTOPIA LENTIS
• EMERY-DREIFUSS MUSCULAR DYSTROPHY
• ENCEPHALOCELE
• ENTAMOEBA HISTOLYTICA ENTERITIS
• ENTEROADHERENT COLITIS
• ENTEROHEMORRHAGIC COLITIS
• ENTEROINVASIVE COLITIS
• ENTEROPATHIC ARTHRITIS
• ENTEROPATHOGENIC ENTERITIS
• ENTEROTOXIGENIC COLITIS
• ENURESIS
• EOSINOPHILIC GASTROENTERITIS
• EPENDYMOMAS
• EPIGLOTTITIS
• ERYTHEMA MUTIFORME MINOR
• ERYTHEMA NODOSUM
• ERYTHEMA TOXICUM NEONATORUM
• ESSENTIAL TREMOR
• EVENTRATION OF THE DIAPHRAGM                                                          
• FABRY DISEASE
• FACTOR XII DEFICIENCY
• FAMILIAL HYPOPHOSPHATEMIA
• FAMILIAL PAROXYSMAL CHOREOATHETOSIS
• FAMILIAL POLYPOSIS COLI
• FANCONI ANEMIA
• FANCONI SYNDROME - RENAL
• FARBER DISEASE
• FEBRILE SEIZURES
• FELTY'S SYNDROME
• FEMORAL ANTEVERSION
• FIFTH DISEASE
• FLAT FEET (FLEXIBLE)
• FLOPPY INFANT
• FORBES DISEASE - GLYCOGENOSIS III
• FRAGILE X SYNDROME
• FRIEDREICH ATAXIA
• FRUCTOSE-1,6-DIPHOSPHATASE DEFICIENCY
• FUCOSIDOSIS
• GALACTOSEMIA-I
• GALACTOSEMIA-II
• GALACTOSEMIA-III
• GALACTOSIALIDOSIS
• GARDNER'S SYNDROME
• GASTROESOPHAGEAL REFLUX DISEASE
• GASTROINTESTINAL POLYPOSIS
• GASTROSCHISIS
• GAUCHER'S DISEASE
• GERM CELL TUMORS
• GIARDIA LAMBLIA ENTERITIS
• GILBERT SYNDROME
• GLUTARIC ACIDEMIA I
• GM1 GANGLIOSIDOSES
• GOLDENHAR SYNDROME
• GONOCCOCAL CONJUNCTIVITIS
• GOODPASTURE'S DISEASE
• GRANULOMA ANNULARE
• GRAVES' DISEASE                                                                                     
• GROWTH HORMONE DEFICIENCY
• GUILLAIN-BARRE SYNDROME
• HALLERVORDEN-SPATZ DISEASE
• HAND-FOOT-AND-MOUTH DISEASE
• HARDING ATAXIA
• HARTNUP DISEASE
• HAWKINSINURIA
• HEADACHE - RECURRENT
• HEARING LOSS
• HEMATURIA
• HEMOLYTIC UREMIC SYNDROME
• HUS COLITIS
• HEMOPHILIA A
• HEMOPHILIA B (CHRISTMAS DISEASE)
• HEMOPHILIA C
• HEMORRHAGIC DISEASE OF THE NEWBORN
• HENOCH-SCHOENLEIN PURPURA
• HSP COLITIS
• HEPATITIS A
• HEPATITIS B
• HEPATITIS C
• HEPATITIS D
• HEPATITIS E
• HEPATOBLASTOMA
• HEPATOCELLULAR CARCINOMA
• HEPATOMEGALY
• HEREDITARY ANGIOEDEMA
• HEREDITARY FRUCTOSE INTOLERANCE
• HERS DISEASE - GLYCOGENOSIS VI
• HIDROTIC ECTODERMAL DYSPLASIA
• HIRSCHSPRUNG DISEASE
• HODGKIN'S LYMPHOMA
• HOLOPROSENCEPHALY
• HOMOCYSTINURIA-I
• HUNTER SYNDROME
• HUNTINGTON'S DISEASE (WESTPHAL VARIANT)
• HURLER SYNDROME
• HYDROCARBON TOXICITY
• HYDROCELE
• HYPERAMMONEMIA
• HYPERTENSION - MALIGNANT                                                                      
• HYPERTENSION - CHRONIC SUSTAINED
• HYPERTHYROIDISM
• HYPERVITAMINOSIS A
• HYPERVITAMINOSIS D
• HYPOCHONDROPLASIA
• HYPOGLYCEMIA
• HYPOHIDROTIC (ANHIDROTIC) ECTODERMAL DYSPLASIA
• HYPOTHALAMIC HAMARTOMAS
• IDIOPATHIC THROMBOCYTOPENIA PURPURA (ITP)
• IDIOPATHIC TORSION DYSTONIA
• IgA NEPHROPATHY (BERGER NEPHROPATHY)
• IMMUNOPROLIFERATIVE SMALL INTESTINAL DISEASE
• INCONTINENTIA PIGMENTI
• INFANTILE SPASMS (WEST SYNDROME)
• INNOCENT HEART MURMURS
• INTESTINAL LYMPHANGIECTASIA
• IRRITABLE BOWEL SYNDROME (IBS)
• ISOLATED JUVENILE POLYPS
• ISOVALERIC ACIDEMIA
• JAUNDICE - NEONATAL
• JOB SYNDROME
• JUVENILE ANKYLOSING SPONDYLITIS
• JUVENILE DERMATOMYOSTITIS
• JUVENILE LARYNGEAL PAPILLOMATOSIS
• JUVENILE POLYPOSIS COLI
• JUVENILE POLYPOSIS OF INFANCY
• JUVENILE RETINOSCHISIS
• KALLMANN SYNDROME
• KAWASAKI'S SYNDROME
• KENNEDY'S DISEASE
• KING SYNDROME
• KLIPPEL-TRENAUNAY-WEBER SYNDROME
• KLUMPKE PARALYSIS
• KOSTMANN AGRANULOCYTOSIS
• KUGELBERG-WELANDER DISEASE                                                                        
• LABIAL FUSION
• LAFORA-BODY DISEASE
• LARYNGEAL FOREIGN BODY
• LARYNGEAL HEMANGIOMA
• LARYNGEAL WEB
• LARYNGOCELE
• LARYNGOMALACIA
• LARYNGOTRACHEOESOPHAGEAL CLEFT
• LAURENCE-MOON SYNDROME
• LCAD DEFICIENCY
• LEGG-CALVE-PERTHES DISEASE
• LENNOX-GASTAUT SYNDROME
• LESCH-NYHAN SYNDROME
• LIMP
• LINEAR NEVUS SYNDROME
• LISSENCEPHALY
• LISTERIOSIS MENINGITIS
• LOCALIZED SCLERODERMA
• LOWE (OCULO-CEREBRO-RENAL) SYNDROME
• LUCEY-DRISCOLL SYNDROME
• LYME DISEASE
• MACHADO-JOSEPH DISEASE
• MACROGYRIA
• MALABSORPTIVE DISORDERS
• MALIGNANT HYPERTHERMIA
• MALROTATION
• MAPLE SYRUP URINE DISEASE (MSUD)
• MAROTEAUX-LAMY SYNDROME
• MAY-HEGGLIN ANOMALY
• MCAD DEFICIENCY
• MCARDLE DISEASE - GLYCOGENOSIS V
• McCUNE-ALBRIGHT SYNDROME
• MECKEL-GRUBER SYNDROME
• MEDIAL TIBIAL TORSION
• MEDULLARY CYSTIC KIDNEY
• MEDULLOBLASTOMA
• MENINGOCELE
• MENINGOCOCCEMIA
• MENKES (KINKY HAIR) DISEASE
• METABOLIC ACIDOSIS
• METACHROMATIC LEUKODYSTROPHY
• METATARSUS ADDUCTUS                                                                                  
• METATARSUS VARUS
• METATROPIC DYSPLASIA
• MICROCEPHALY
• MICROGYRIA
• MIGRAINE
• MIGRAINE VARIANT - THE RUSHES
• MILLER-FISHER SYNDROME
• MOEBIUS SYNDROME
• MOLLUSCUM CONTAGIOSUM
• MONONUCLEOSIS
• MORQUIO SYNDROME
• MUCOPOLYSACCHARIDOSIS
• MULTIPLE EPIPHYSEAL DYSPLASIA
• MULTIPLE SCLEROSIS
• MYELOMENINGOCELE
• MYELOPEROXIDASE DEFICIENCY
• MYELOSCHISIS
• MYOCLONUS EPILEPSY AND RAGGED-RED FIBRES (MERRF)
• MYOTONIC DYSTROPHY
• MYOTUBULAR MYOPATHY - X-LINKED
• NAIL-PATELLA SYNDROME
• NASAL POLYPS
• NEMALINE ROD MYOPATHY
• NEONATAL GRAVES' DISEASE
• NEONATAL HEPATITIS
• NEONATAL SEIZURES
• NEPHROGENIC DIABETES INSIPIDUS
• NEPHROTIC SYNDROME - IDIOPATHIC
• NEPHROTIC SYNDROME - CONGENITAL
• NEUROBLASTOMA
• NEUROFIBROMATOSIS (TYPE 1)
• NEURONAL CEROID-LIPOFUSCINOSES
• NEURONAL MIGRATION DISORDERS
• NIGHT TERRORS
• NON-HODGKIN'S LYMPHOMA
• NON-KETOTIC HYPERGLYCINEMIA
• NOONAN SYNDROME
• NORRIE DISEASE                                                                                                        
• NORWALK ENTERITIS
• NSP OF INTERLOBULAR BILE DUCTS
• OCCIPITAL HORN SYNDROME
• OMENN DISEASE
• OMPHALOCELE
• OPITZ-FRAIS SYNDROME
• ORNITHINE TRANSCARBAMYLASE (OTC) DEFICIENCY
• OROTIC ACIDURIA
• ORTHOSTATIC PROTEINURIA
• OSGOOD-SCHLATTER DISEASE
• OSTEOCHONDRITIS DISSECANS
• OSTEOCHONDROMA
• OSTEOID OSTEOMA
• OSTEOSARCOMA
• OTITIS MEDIA
• PALLISTER-KILLIAN MOSAIC SYNDROME
• PAROXYSMAL NOCTURNAL HEMOGLOBINURIA
• PATENT DUCTUS ARTERIOSUS
• PELIZAEUS-MERZBACHER DISEASE
• PENDRED SYNDROME
• PEPTIC ULCER DISEASE
• PERITONSILLAR ABSCESS
• PERSISTENT ASYMPTOMATIC PROTEINURIA
• PERTUSSIS (WHOOPING COUGH)
• PEUTZ-JEGHERS SYNDROME
• PFEIFFER SYNDROME
• PIERRE ROBIN SYNDROME
• PINWORM
• PITYRIASIS (TINEA) VERSICOLOR
• PITYRIASIS ROSEA
• PITYRIASIS RUBRA PILARIS
• PNEUMONIA - BACTERIAL
• PNEUMONIA - GROUP A STREPTOCOCCAL
• PNEUMONIA - HAEMOPHILUS INFLUENZAE
• PNEUMONIA - PNEUMOCOCCAL
• PNEUMONIA - STAPHYLOCOCCAL
• PNEUMOTHORAX
• PNEUMOTHORAX - NEONATAL
• POLYCYSTIC KIDNEY DISEASE - INFANTILE FORM
• PORENCEPHALY
• POSTSTREPTOCOCCAL GLOMERULONEPHRITIS
• PRADER-WILLI SYNDROME
• PRECOCIOUS PUBERTY - CEREBRAL
• PRECOCIOUS PUBERTY - CONSTITUTIONAL
• PRIMARY CILIARY DYSKINESIS
• PROGRESSIVE MYOCLONUS EPILEPSIES
• PROGRESSIVE RUBELLA PANENCEPHALITIS (PRP)
• PROGRESSIVE SYSTEMIC SCLEROSIS
• PROPIONIC ACIDEMIA
• PROTEINURIA
• PRUNE BELLY SYNDROME
• PSEUDOMEMBRANOUS COLITIS                                                                      
• PSEUDOTUMOR CEREBRI
• PSORIASIS
• PSORIATIC SPONDYLOARTHRITIS
• PULMONARY SEQUESTRATION
• PYRIDOXINE DEFICIENCY
• PYROGLUTAMIC ACIDEMIA
• PYRUVATE DECARBOXYLASE DEFICIENCY
• RASMUSSEN'S ENCEPHALITIS
• RECURRENT ABDOMINAL PAIN
• REFSUM DISEASE
• REITER'S DISEASE
• RETT SYNDROME
• RHABDOMYOSARCOMA
• RHINITIS - ALLERGIC
• RHINITIS - VASOMOTOR
• RILEY-DAY SYNDROME
• ROTAVIRUS ENTERITIS
• ROTOR SYNDROME
• RUBINSTEIN-TAYBI SYNDROME
• SALICYLATE OVERDOSE
• SANDHOFF DISEASE
• SANFILIPPO A SYNDROME
• SARCOSINEMIASCABIES
• SCAD DEFICIENCY
• SCHEIE SYNDROME
• SCHINDLER DISEASE
• SCHIZENCEPHALY
• SELECTIVE IgA DEFICIENCY
• SELECTIVE IgM DEFICIENCY
• SEPTIC ARTHRITIS
• SERONEGATIVE SPONDYLOARTHROPATHIES
• SEVERE COMBINED IMMUNODEFICIENCY DISEASE
• SEVERE COMBINED IMMUNODEFICIENCY DISEASE (SCID)- IL-2
• SHIGELLOSIS COLITIS
• SHORT BOWEL SYNDROME
• SHORT RIB-POLYDACTYLY SYNDROME
• SHORT STATURE
• SHWACHMAN-DIAMOND SYNDROME
• SIALIDOSIS
• SIMPLE PARTIAL SEIZURES (SPS)
• SINUSITIS                                                                                                          
• SLEEPWALKING
• SLIPPED CAPITAL FEMORAL EPIPHYSIS
• SLY SYNDROME
• SOTO SYNDROME
• SPECIFIC GRANULE DEFICIENCY
• SPINA BIFIDA OCCULTA
• SPINAL MUSCULAR ATROPHY - INTERMEDIATE FORM
• SPINOCEREBELLAR ATAXIA - TYPE 1
• SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA
• STAGNANT LOOP SYNDROME
• STATUS EPILEPTICUS
• STRABISMUS
• STURGE-WEBER SYNDROME
• STYE (HORDEOLUM)
• SUBACUTE SCLEROSING PANENCEPHALITIS
• SUBGLOTTIC STENOSIS
• SULFITE OXIDASE DEFICIENCY
• SYDENHAM'S CHOREA
• SYSTEMIC LUPUS ERYTHROMATOSUS
• TAR SYNDROME
• TARUI DISEASE - GLYCOGENOSIS VII
• TAY SACHS DISEASE
• TELOGEN EFFLUVIUM
• TEMPER TANTRUMS
• TETRALOGY OF FALLOT
• THALASSEMIA - BETA
• THANATOPHORIC DYSPLASIA
• THIN GLOMERULAR BASEMENT MEMBRANE DISEASE
• THOMSEN'S DISEASE (MYOTONIA CONGENITA)
• THYROIDITIS
• TIC DISORDERS
• TODDLER DIARRHEA
• TOURETTE SYNDROME
• TOWNES-BROCKS SYNDROME
• TRACHEAL AMYLOIDOSIS
• TRACHEOMALACIA
• TRANSIENT ERYTHROBLASTOPENIA OF CHILDHOOD
• TRANSIENT HYPERAMMONEMIA OF THE NEWBORN (THAN)
• TRANSIENT HYPOGAMMAGLOBULINEMIA OF INFANCY
• TRANSIENT SYNOVITIS
• TRANSIENT TIC DISORDER
• TRANSIENT TYROSINEMIA OF THE NEWBORN                                                    
• TRANSPOSITION OF THE GREAT ARTERIES
• TREACHER COLLINS SYNDROME
• TRIMETHYLAMINURIA
• TRISOMY 13 SYNDROME
• TRISOMY 18 SYNDROME
• TROPICAL SPRUE
• TUBEROUS SCLEROSIS
• TURCOT'S SYNDROME
• TURNER SYNDROME
• TYROSINEMIA-I
• TYROSINEMIA-II
• ULCERATIVE COLITIS
• UMBILICAL HERNIA
• UNVERRICHT-LUNDBORG DISEASE
• URINARY TRACT INFECTIONS
• URTICARIA (HIVES)
• VACTERL ASSOCIATION
• VENTRICULAR SEPTAL DEFECT
• VIBRIO CHOLERAE
• VISCERAL LARVA MIGRANS
• VON GIERKE DISEASE - GLYCOGENOSIS Ia
• VON HIPPEL-LINDAU DISEASE
• VON WILLEBRAND DISEASE - TYPE 1
• WAARDENBURG SYNDROMES
• WEAVER SYNDROME
• WERDNIG-HOFFMANN DISEASE
• WHIPPLES DISEASE
• WILLIAMS SYNDROME
• WILMS' TUMOR
• WILSON'S DISEASE
• WISKOTT-ALDRICH SYNDROME
• WOLF SYNDROME
• WOLMAN DISEASE
• XERODERMA PIGMENTOSUM
• XXX SYNDROME
• XXXX SYNDROME
• XXXXX SYNDROME
• YERSINIA ENTEROCOLITICA
• ZELLWEGER'S SYNDROME