GuidaMacropolis

 


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