The Pediatric Database (PEDBASE) contains descriptions of over 500 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 updated Registered version is also available through the author.
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
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
DISLOCATION OF THE HIP
CONGENITAL
DYSERYTHROPOIETIC ANEMIA
CONGENITAL
HSV
CONGENITAL
HYPOTHYROIDISM
CONGENITAL
LOBAR EMPHYSEMA
CONGENITAL
MESOBLASTIC NEPRHOMA
CONGENITAL
MUSCLE FIBRE-TYPE DISPROPORTION
CONGENITAL
MUSCULAR DYSTROPHY
CONGENITAL
NEPHROTIC SYNDROME
CONGENITAL
PULMONARY LYMPHANGECTASIA
CONGENITAL
RUBELLA
CONGENITAL
TOXOPLASMOSIS
CONGENITAL
VARICELLA
CONSTIPATION
CORNELIA
DE LANGE SYNDROME
COWDEN'S
SYNDROME
CRANIOSYNOSTOSIS
CRIGLER-NAJJAR
SYNDROME - I
CROHN'S
DISEASE
CROUP
CROUZON
SYNDROME
CRYPTORCHIDISM
CRYPTOSPORIDIUM
ENTERITIS
CYCLIC
NEUTROPENIA
CYSTIC
ADENOMATOID MALFORMATION
CYSTIC
FIBROSIS
CYSTINOSIS
CYSTINURIA
DANDY-WALKER
MALFORMATION
DEJERINE-SOTTAS
DISEASE
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
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
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
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
GM1
GANGLIOSIDOSES
GONOCCOCAL
CONJUNCTIVITIS
GOODPASTURE'S
DISEASE
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
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
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
NEPHROTIC SYNDROME
IDIOPATHIC
THROMBOCYTOPENIA PURPURA (ITP)
IDIOPATHIC
TORSION DYSTONIA
IgA
NEPHROPATHY (BERGER NEPHROPATHY)
IMMUNOPROLIFERATIVE
SMALL INTESTINAL DISEASE
INCONTINENTIA
PIGMENTI
INFANTILE
SPASMS (WEST SYNDROME)
INNOCENT
HEART MURMERS
INTESTINAL
LYMPHANGIECTASIA
IRRITABLE
BOWEL SYNDROME (IBS)
ISOLATED
JUVENILE POLYPS
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
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
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
MILLER-FISHER
SYNDROME
MOEBIUS
SYNDROME
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
NEUROBLASTOMA
NEUROFIBROMATOSIS
(TYPE 1)
NEURONAL
CEROID-LIPOFUSCINOSES
NEURONAL
MIGRATION DISORDERS
NIGHT
TERRORS
NON-HODGKIN'S
LYMPHOMA
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
PAROXYSMAL
NOCTURNAL HEMOGLOBINURIA
PATENT
DUCTUS ARTERIOSUS
PELIZAEUS-MERZBACHER
DISEASE
PEPTIC
ULCER DISEASE
PERITONSILLAR
ABSCESS
PERSISTENT
ASYMPTOMATIC PROTEINURIA
PERTUSSIS
(WHOOPING COUGH)
PEUTZ-JEGHERS
SYNDROME
PFEIFFER
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
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
SCABIES
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
SUBACUTE
SCLEROSING PANENCEPHALITIS
SUBGLOTTIC
STENOSIS
SULFITE
OXIDASE DEFICIENCY
SYDENHAM'S
CHOREA
SYSTEMIC
LUPUS ERYTHROMATOSUS
TAR
SYNDROME
TARUI
DISEASE - GLYCOGENOSIS VII
TAY
SACHS DISEASE
TEMPER
TANTRUMS
TETRALOGY
OF FALLOT
THALASSEMIA
- BETA
THANATOPHORIC
DWARFISM
THIN
GLOMERULAR BASEMENT MEMBRANE DISEASE
THOMSEN'S
DISEASE (MYOTONIA CONGENITA)
THYROIDITIS
TIC
DISORDERS
TODDLER
DIARRHEA
TOURETTE
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
TRISOMY
13 SYNDROME
TRISOMY
18 SYNDROME
TROPICAL
SPRUE
TUBEROUS
SCLEROSIS
TURCOT'S
SYNDROME
TURNER
SYNDROME
TYROSINEMIA-I
TYROSINEMIA-II
ULCERATIVE
COLITIS
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
DISEASE
WISKOTT-ALDRICH
SYNDROME
WOLF
SYNDROME
WOLMAN
DISEASE
XERODERMA
PIGMENTOSUM
YERSINIA
ENTEROCOLITICA
ZELLWEGER'S
SYNDROME