Pedbase Site Map
Pediatric
Site Map
Resources
Contact
PEDBASE.org - The Pediatric Database
A
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
CEREBELLAR VERMIS
AGENESIS OF THE CORPUS CALLOSUM
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 CRISIS
APLASTIC ANEMIA
ARGININEMIA
ARGININOSUCCINIC ACIDURIA
ASPHYXIATING THORACIC DYSTROPHY
ASTHMA - ALLERGIC
ASTHMA - ACUTE
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
B
BACTERIAL TRACHEITIS
BACTERIAL MENINGITIS
BARAKAT'S SYNDROME
BECKER MUSCULAR DYSTROPHY
BECKWITH-WIEDEMANN SYNDROME
BELL'S PALSY
BENIGN CONGENITAL HYPOTONIA
BENIGN FAMILIAL NEONATAL SEIZURES
BENIGN FAMILIAL HEMATURIA
BENIGN FRUCTOSURIA
BENIGN HEREDITARY CHOREA
BENIGN PARTIAL EPILEPSY WITH CENTROTEMPORAL SPIKES (BPEC)
BENIGN PAROXYSMAL VERTIGO
BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS
BENIGN TRANSIENT PROTEINURIA
BERNARD-SOULIER SYNDROME
BLASTOCYSTIS HOMINIS ENTERITIS
BLOCKED TEAR DUCT (DACRYOSTENOSIS)
BLOOM SYNDROME
BRAIN STEM GLIOMA
BRONCHIOLITIS OBLITERANS
BRONCHIOLITIS - ACUT
E
BRONCHOGENIC CYSTS
BRUTON DISEASE
BYLER DISEASE
C
CAFFEY DISEASE
CALICIVIRUS ENTERITIS
CAMPYLOBACTER ENTEROCOLITIS
CANAVAN'S DISEASE
CARBAMOYL PHOSPHATE SYNTHETASE (CPS) DEFICIENCY
CARDIO-FACIAL-CUTANEOUS (CFC) SYNDROME
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 MUCOCUTANEOUS CANDIDIASIS
CHRONIC BRONCHITIS
CHRONIC COUGH
CHRONIC GRANULOMATOUS DISEASE - X-LINKED
CHRONIC MOTOR OR VOCAL TIC DISORDER
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 BRONCHOBILIARY FISTULA
CONGENITAL CMV
CONGENITAL DYSERYTHROPOIETIC ANEMIA
CONGENITAL HSV
CONGENITAL HYPOTHYROIDISM
CONGENITAL LOBAR EMPHYSEMA
CONGENITAL MESOBLASTIC NEPHROMA
CONGENITAL MUSCLE FIBRE-TYPE DISPROPORTION
CONGENITAL MUSCULAR DYSTROPHY
CONGENITAL PULMONARY LYMPHANGECTASIA
CONGENITAL RUBELLA
CONGENITAL TOXOPLASMOSIS
CONGENITAL VARICELLA
CONGENITAL PARVOVIRUS B19
CONSTIPATION
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
D
DANDY-WALKER MALFORMATION
DEJERINE-SOTTAS DISEASE
DEVELOPMENTAL DYSPLASIA OF THE HIP
DIABETIC KETOACIDOSIS (DKA)
DIAMOND-BLACKFAN SYNDROME
DIAPHYSEAL DYSPLASIA
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
E
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 MULTIFORME MINOR
ERYTHEMA NODOSUM
ESSENTIAL TREMOR
EVENTRATION OF THE DIAPHRAGM
ERYTHEMA TOXICUM NEONATORUM
F
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
G
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
GRAVES' DISEASE
GROWTH HORMONE DEFICIENCY
GUILLAIN-BARRE SYNDROME
H
HALLERVORDEN-SPATZ DISEASE
HAND-FOOT-AND-MOUTH DISEASE
HARDING ATAXIA
HARTNUP DISEASE
HAWKINSINURIA
HEADACHE - RECURRENT
HEARING LOSS
HEMATURIA
HEMOLYTIC UREMIC SYNDROME
HEMOLYTIC UREMIC SYNDROME COLITIS
HEMOPHILIA A
HEMOPHILIA B (CHRISTMAS DISEASE)
HEMOPHILIA C
HEMORRHAGIC DISEASE OF THE NEWBORN
HENOCH-SCHOENLEIN PURPURA
HENOCH-SCHOENLEIN PURPURA 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
I
IDIOPATHIC THROMBOCYTOPENIC 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
J
JAUNDICE - NEONATAL
JOB SYNDROME
JUVENILE ANKYLOSING SPONDYLITIS
JUVENILE DERMATOMYOSTITIS
JUVENILE LARYNGEAL PAPILLOMATOSIS
JUVENILE POLYPOSIS COLI
JUVENILE POLYPOSIS OF INFANCY
JUVENILE RETINOSCHISIS
K
KALLMANN SYNDROME
KAWASAKI SYNDROME
KENNEDY'S DISEASE
KING SYNDROME
KLIPPEL-TRENAUNAY-WEBER SYNDROME
KLUMPKE PARALYSIS
KOSTMANN AGRANULOCYTOSIS
KUGELBERG-WELANDER DISEASE
L
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
M
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