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DATA BASE PEDIATRICO
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.
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 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 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 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 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 HEAD LICE 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 POLAND SYNDROME 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 SARCOSINEMIA SCABIES SCAD DEFICIENCY SCHEIE SYNDROME SCHINDLER DISEASE SCHIZENCEPHALY SELECTIVE IgA DEFICIENCY SELECTIVE IgM DEFICIENCY SEPTIC ARTHRITIS SERONEGATIVE SPONDYLOARTHROPATHIES SEVER'S DISEASE 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 SMITH-LEMLI-OPITZ SYNDROME SOTOS SYNDROME SPECIFIC GRANULE DEFICIENCY SPINA BIFIDA OCCULTA SPINAL MUSCULAR ATROPHY - INTERMEDIATE FORM SPINOCEREBELLAR ATAXIA - TYPE 1 SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA SPRENGEL'S DEFORMITY 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