| Cardiovascular
|
Atrioventricular septal defect , BlandGarlandWhite syndrome , Congenital heart disease, Cor Triatriatum , Double outlet right ventricle , Endocardial fibroelastosis , Fallot's tetralogy, Patent ductus arteriosus, Transposition of great arteries , Ventricular septal defect
|
| Chemical / poisoning
|
Lead poisoning
|
| Dermatologic
|
Leiner Disease
|
| Drug Side Effect
|
Fetal Hydantoin Syndrome , Fetal thalidomide syndrome , Fetal warfarin syndrome , Prednisolone
|
| Ear Nose Throat
|
No underlying causes
|
| Endocrine
|
Adiposogenital dystrophy, Adrenal hyperplasia, congenital type 3 , Adrenomyodystrophy , C21 hydroxylase deficiency, Cushing's syndrome , Cystic fibrosis , Diabetes mellitus, Glucocorticoid deficiency, Growth hormone deficiency, Hyperthyroidism, Hypoaldosteronism, Hypopituitarism , Hypothyroidism, KaplowitzBodurtha syndrome , Pseudohypoparathyroidism , Thyroid disease
|
| Environmental
|
Lead poisoning
|
| Gastroenterologic
|
Autoimmune enteropathy , Baber's syndrome , Bile acid synthesis defects , Blind loop syndrome , Chronic diarrhoea, Congenital short bowel , Congenital Vitamin B12 Malabsorption , Glucosegalactose malabsorption , Hirschsprung's disease , Malabsorption syndrome, Microvillus Inclusion Disease , Pseudoobstruction idiopathic intestinal
|
| Genetic
|
14q+ syndrome , 18 Hydroxylase deficiency , 18p minus syndrome , 1q deletion , 2q deletion , 3M syndrome , 3q deletion , 49,XXXXX syndrome , 4p16.3 deletion , Aarskog syndrome , Aase syndrome, Abetalipoproteinaemia, ACAD8 deficiency , Adiposogenital dystrophy, Alagille Syndrome , AlbersSchonberg disease , Albright's hereditary osteodystrophy , AlphaLiduronidase deficiency, Alport Syndrome , Alports syndrome, Alsing syndrome , Aminomethyltransferase deficiency, Andersen disease , Anorexia nervosa, Arginase deficiency , Aspartoacylase deficiency, BardetBiedl syndrome, Barth syndrome , Bloom's syndrome, BonnetDechaumeBlanc syndrome, BowenConradi syndrome , BRESHECK syndrome, Byler Disease , CAH, CAMFAK syndrome , Campomelic dwarfism , Carnitine transporter deficiency , Carnosinase deficiency , Carpenter syndrome , CHARGE syndrome, Chromosome 1 uniparental disomy 1q12 q21 , Chromosome 10 ring syndrome , Chromosome 10, distal trisomy 10q , Chromosome 10p deletion syndrome , Chromosome 11q duplication syndrome , Chromosome 12 ring syndrome , Chromosome 12p deletion , Chromosome 13 ring syndrome , Chromosome 13 trisomy syndrome , Chromosome 14 Ring , Chromosome 14 trisomy , Chromosome 15 trisomy , Chromosome 16p, partial duplication , Chromosome 17 ring , Chromosome 18 Ring , Chromosome 19 ring syndrome , Chromosome 1p deletion syndrome , Chromosome 2 trisomy syndrome , Chromosome 20 ring , Chromosome 20p deletion syndrome , Chromosome 21 monosomy , Chromosome 22, trisomy , Chromosome 2p deletion syndrome , Chromosome 2p duplication syndrome , Chromosome 3, trisomy 3p , Chromosome 3, trisomy 3q , Chromosome 4 Ring , Chromosome 4 ring syndrome , Chromosome 5, trisomy 5q , Chromosome 5p duplication syndrome , Chromosome 5p tetrasomy syndrome , Chromosome 6 ring syndrome , Chromosome 6, monosomy 6q , Chromosome 6, trisomy 6q , Chromosome 7 ring syndrome , Chromosome 8 recombinant syndrome , Chromosome 9 trisomy syndrome , Chromosome 9, trisomy , Classic galactosemia , Cleft palate, Cockayne syndrome, CoffinLowry syndrome, Cohen Syndrome , Complement 5 deficiency, Complete Trisomy 18 syndrome , Complex 5 mitochondrial respiratory chain deficiency , Congenital chloride diarrhea , ConradiHuenermann Syndrome , Corpus callosum agenesis , Criduchat syndrome , De Barsy syndrome, DiamondBlackfan anemia , DiGeorge syndrome , Down syndrome, Edward Syndrome , Faciocardiorenal syndrome, Fallot's tetralogy, Farber's disease , Filippi syndrome, Forbes disease , Francois dyscephalic syndrome , Fucosidosis, Galactosemia , GAPO syndrome , Glucosegalactose malabsorption , HoyeraalHreidarsson syndrome , ICF syndrome , Iduronate sulphatase deficiency, Inborn amino acid metabolism disorder , Inborn urea cycle disorder , Infantile dysphagia , Infantile hypophosphatasia , Infantile Refsum Disease , IPEX syndrome , Ivemark Syndrome , Jeune's thoracic dystrophy syndrome, JirasekZuelzerWilson syndrome , JohansonBlizzard syndrome, JubergMarsidi syndrome , Kabuki makeup syndrome, Kartagener's syndrome, KennyCaffeyLinarelli syndrome, Kowarski syndrome , Leigh syndrome , Leprechaunism, LeriWeill dyschondrosteosis, Lissencephaly , Lissencephaly, Lowe oculocerebrorenal syndrome , Lowe Syndrome , LutzRichnerLandolt syndrome , Maple syrup urine disease, MardenWalker syndrome, Martsolf syndrome, Menkes Disease , Miescher's syndrome , Mitochondrial diseases, MULIBREY Nanism , Multiple lentigines syndrome, Navajo neurohepatopathy , Neuronal Migration Disorders , Nezelof Syndrome , NiemannPick disease , NOMID syndrome , Omenn syndrome , Opitz trigonocephaly syndrome, Osteogenesis imperfecta, Otopalatodigital syndrome, Pearson's anemia , PelizaeusMerzbacher disease, Phenylketonuria , Pierre Robin's sequence , PittRogersDanks syndrome, Pompe disease , PowellBuistStenzel syndrome , PraderWilli syndrome , Progeroid syndrome, Progressive familial intrahepatic cholestasis, RussellSilver dwarfism, SaethreChotzen Syndrome , SCID , Seckle syndrome , Sheffield syndrome , ShwachmanDiamond Syndrome , Sickle Cell Anemia , Silver's syndrome, SingletonMerten Syndrome , TaySachs disease, Thyroid agenesis , Transposition of great arteries , Trisomy 18 Syndrome , Turner syndrome , Tyrosinemia , VATER association , Velocardiofacial syndrome, Von Gierke disease , WAGR Syndrome , Watson syndrome , Williams syndrome, Wittwer sydnrome , WolcottRallison syndrome , YunisVaron syndrome, ZAP70 deficiency
|
| Hematologic
|
Fanconi syndrome , Acanthocytosis , Agammaglobulinemia, alymphocytotic type , Angiofollicular lymph hyperplasia , Athymia, Bare lymphocyte syndrome , CMLLike Syndrome, Familial , Haemoglobin E disease, Hemophagocytic reticulosis , Histiocytosis X, Langerhans Cell Histiocytosis , Severe combined immunodeficiency , Thalassemia
|
| Iatrogenic
|
No underlying causes
|
| Infectious Disease
|
AIDS , Ascariasis, Chronic urinary tract infections, Chronic viral infection, Congenital syphilis , Congenital tuberculosis , Mycobacterium tuberculosis, Parasite infestation, Tuberculosis
|
| Musculoskeletal / Ortho
|
Cantu syndrome, CareyFinemanZiter syndrome, Osteopetrosis with renal tubular acidosis , BallerGerold syndrome, FreemanSheldon Syndrome postnatal growth deficiency, Phocomelia syndrome
|
| Neurologic
|
HoyeraalHreidarsson syndrome , Ramon syndrome, Rieger Syndrome , Agyria , Alpers Syndrome , Cerebral palsy, Crome syndrome, Diencephalic Syndrome , Encephaloceles , Frynsvan den Berghe syndrome, Gangliosidosis, Hooft disease growth delay
|
| Nutritional / Metabolic
|
GraeckImerslund disease , Abetalipoproteinaemia, Anorexia nervosa, Forbes disease , Fucosidosis, Galactosemia , Menkes Diseas, , Osteomalacia, Rumination disorder , Food intolerances, Heiner syndrome , 3methylglutaconic aciduria, type 4 , 4Alphahydroxyphenylpyruvate hydroxylase deficiency , 4hydroxyphenylpyruvate hydroxylase deficiency, Acrodermatitis enteropathica , AcylCoA dehydrogenase, short chain, deficiency of , Adenylosuccinate lyase deficiency , Arterial occlusive disease, Chylomicron retention disease, Cystinosis , Dietary deficiencies, Gaucher's disease, GlutarylCoA dehydrogenase deficiency , Glycerol kinase deficiency, GRACILE syndrome, Gylcogen storage disease, Hemosiderosis , Hurler syndrome , Icell disease, Kwashiorkor, Lipoproteine lipase deficiency , Marasmus , MELAS, Methylmalonic acidemia , Nutritional deficiency , Zinc deficiency
|
| Obstetric/Gynecologic
|
Toxoplasmosis, Rubella, Cytomegalovirus, HSV
|
| Oncologic
|
Juvenile myelomonocytic leukemia , Leukemia
|
| Opthalmologic
|
No underlying causes
|
| Overdose / Toxicity
|
No underlying causes
|
| Psychiatric
|
No underlying causes
|
| Pulmonary
|
Asthma, Bronchiectasis, Congenital pulmonary alveolar proteinosis , Pulmonary veins stenosis
|
| Renal / Electrolyte
|
Nephrogenic diabetes insipidus , Aspartylglucosaminuria, Bartter Syndrome , Chronic renal failure, Classic Distal Renal Tubular Acidosis , Hypophosphatasia , Renal failure, LightwoodAlbright syndrome , Nephrotic syndrome, Primary tubular proximal acidosis
|
| Rheum / Immune / Allergy
|
Crohn's disease, Inflammatory bowel disease, Majeed syndrome , Celiac disease
|
| Sexual
|
No underlying causes
|
| Trauma
|
No underlying causes
|
| Urologic
|
No underlying causes
|
| Dental
|
No underlying causes
|
| Miscellaneous
|
Abnormal feeding habits, Child abuse, Neglect, Starvation
|