Jaundice
Symptom Information:
Symptom ID: | HPO:0000952 | |||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the liver(HPO:0001392) Abnormality of the biliary system(HPO:0004297) Cholestasis(HPO:0001396) Jaundice(HPO:0000952) Abnormality of the integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Generalized abnormality of skin(HPO:0011354) Dermatological manifestations of systemic disorders(HPO:0001005) Jaundice(HPO:0000952) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Haemolyses and related conditions(MedDRA:10018911) Haemolyses NEC(MedDRA:10018913) Jaundice(HPO:0000952) |
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Database Frequency: | 105 / 7739 | |||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ACETAMINOPHEN METABOLISM | (OMIM:100675) |
ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib | (OMIM:615631) |
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, POSSIBLY DUE TO DEFECT IN PORPHYRINMETABOLISM | (OMIM:206400) |
ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS | (OMIM:108050) |
ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2 | (OMIM:613404) |
ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3 | (OMIM:170995) |
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins | (Orphanet:217371) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4 | (OMIM:214950) |
BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5 | (OMIM:616278) |
BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY | (OMIM:210550) |
Beckwith-Wiedemann syndrome due to 11p15 microdeletion | (Orphanet:231127) |
Benign recurrent intrahepatic cholestasis type 2 | (Orphanet:99961) |
Biliary atresia | (Orphanet:30391) |
CHOLESTASIS WITH GALLSTONE, ATAXIA, AND VISUAL DISTURBANCE | (OMIM:214980) |
CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3 | (OMIM:614972) |
Cholestasis - lymphedema | (Orphanet:1414) |
Cholestasis - pigmentary retinopathy - cleft palate | (Orphanet:1415) |
Chédiak-Higashi syndrome | (Orphanet:167) |
Congenital bile acid synthesis defect type 1 | (Orphanet:79301) |
Congenital bile acid synthesis defect type 2 | (Orphanet:79303) |
Congenital bile acid synthesis defect type 3 | (Orphanet:79302) |
Congenital dyserythropoietic anemia type II | (Orphanet:98873) |
Congenital dyserythropoietic anemia type III | (Orphanet:98870) |
Congenital intrauterine infection-like syndrome | (Orphanet:1229) |
Constitutional megaloblastic anemia with severe neurologic disease | (Orphanet:319651) |
Crigler-Najjar syndrome | (Orphanet:205) |
Crigler-Najjar syndrome type 2 | (Orphanet:79235) |
DPAGT1-CDG | (Orphanet:86309) |
Dehydrated hereditary stomatocytosis | (Orphanet:3202) |
Dubin-Johnson syndrome | (Orphanet:234) |
EDINBURGH MALFORMATION SYNDROME | (OMIM:129850) |
Familial hemophagocytic lymphohistiocytosis | (Orphanet:540) |
Familial lipoprotein lipase deficiency | (Orphanet:309015) |
Fanconi syndrome - ichthyosis - dysmorphism | (Orphanet:1981) |
Fetal Gaucher disease | (Orphanet:85212) |
GILBERT SYNDROME | (OMIM:143500) |
Galactose epimerase deficiency | (Orphanet:79238) |
Gaucher disease type 2 | (Orphanet:77260) |
Glycogen storage disease due to aldolase A deficiency | (Orphanet:57) |
Glycogen storage disease due to muscle phosphofructokinase deficiency | (Orphanet:371) |
HALOTHANE HEPATITIS | (OMIM:234350) |
HEMOGLOBIN--ALPHA LOCUS 1 | (OMIM:141800) |
HEMOGLOBIN--BETA LOCUS | (OMIM:141900) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 | (OMIM:267700) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 | (OMIM:603553) |
HYPERBILIRUBINEMIA, CONJUGATED, TYPE III | (OMIM:237550) |
HYPERBILIRUBINEMIA, SHUNT, PRIMARY | (OMIM:237800) |
Hemochromatosis, type 1 | (OMIM:235200) |
Hemoglobinopathy Toms River | (Orphanet:280615) |
Hemolytic anemia due to diphosphoglycerate mutase deficiency | (Orphanet:714) |
Hemolytic anemia due to glucophosphate isomerase deficiency | (Orphanet:712) |
Hemolytic anemia due to red cell pyruvate kinase deficiency | (Orphanet:766) |
Hereditary coproporphyria | (Orphanet:79273) |
Hereditary fructose intolerance | (Orphanet:469) |
Hereditary spherocytosis | (Orphanet:822) |
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency | (Orphanet:401948) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Ichthyosis - hypotrichosis - sclerosing cholangitis | (Orphanet:59303) |
Idiopathic copper-associated cirrhosis | (Orphanet:209919) |
JAUNDICE, FAMILIAL OBSTRUCTIVE, OF INFANCY | (OMIM:308600) |
Jeune syndrome | (Orphanet:474) |
Lambert syndrome | (Orphanet:1296) |
Leprechaunism | (Orphanet:508) |
Letterer-Siwe disease | (Orphanet:99870) |
Low phospholipid associated cholelithiasis | (Orphanet:69663) |
MELAS | (Orphanet:550) |
Menkes disease | (Orphanet:565) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
NEUROFIBROMATOSIS-PHEOCHROMOCYTOMA-DUODENAL CARCINOID SYNDROME | (OMIM:162240) |
Navajo neurohepatopathy | (Orphanet:255229) |
Neonatal hemochromatosis | (Orphanet:446) |
Neonatal intrahepatic cholestasis due to citrin deficiency | (Orphanet:247598) |
Niemann-Pick disease type C | (Orphanet:646) |
Non-spherocytic hemolytic anemia due to hexokinase deficiency | (Orphanet:90031) |
PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX | (OMIM:260480) |
PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER) | (OMIM:214110) |
PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER) | (OMIM:614866) |
Pancreatic insufficiency - anemia - hyperostosis | (Orphanet:199337) |
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis | (Orphanet:65288) |
Progressive familial intrahepatic cholestasis | (Orphanet:172) |
Progressive familial intrahepatic cholestasis type 1 | (Orphanet:79306) |
Progressive familial intrahepatic cholestasis type 2 | (Orphanet:79304) |
Progressive familial intrahepatic cholestasis type 3 | (Orphanet:79305) |
RETICULOENDOTHELIOSIS, X-LINKED | (OMIM:312500) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Reticular dysgenesis | (Orphanet:33355) |
Reynolds syndrome | (Orphanet:779) |
Rh deficiency syndrome | (Orphanet:71275) |
Rotor syndrome | (Orphanet:3111) |
SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 1 | (OMIM:109270) |
SPECTRIN, BETA, ERYTHROCYTIC | (OMIM:182870) |
SPHEROCYTOSIS, TYPE 1 | (OMIM:182900) |
Short chain acyl-CoA dehydrogenase deficiency | (Orphanet:26792) |
Short-rib thoracic dysplasia 1 with or without polydactyly | (OMIM:208500) |
Sickle cell anemia | (Orphanet:232) |
Syndromic diarrhea | (Orphanet:84064) |
Transient familial neonatal hyperbilirubinemia | (Orphanet:2312) |
Triose phosphate-isomerase deficiency | (Orphanet:868) |
Tyrosinemia type 1 | (Orphanet:882) |
VISCERAL STEATOSIS, CONGENITAL | (OMIM:228100) |
Wilson disease | (Orphanet:905) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
[DEL] ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1 | (OMIM:208085) |