Jaundice

Symptom Information:

Symptom ID: HPO:0000952
Synonyms:
Icterus [Orphanet:29180]
Jaundice (finding) [Orphanet:29180]
Jaundice [OMIM:Jaundice]
Hepatitis/icterus/cholestasis [Orphanet:29180]
Jaundice [Orphanet:29180]
Jaundice [MedDRA:10023126]
Icterus [MedDRA:10023126]
Jaundice (excl neonatal) [MedDRA:10023126]
Jaundice NOS [MedDRA:10023126]
Jaundice, unspecified, not of newborn [MedDRA:10023126]
Subicteric [MedDRA:10023126]
Icterus [OMIM:Icterus]
Jaundice (1 patient) [OMIM:Jaundice (1 patient)]
Jaundice (harderoporphyria) [OMIM:Jaundice (harderoporphyria)]
Jaundice (in some patients) [OMIM:Jaundice (in some patients)]
Jaundice (in some) [OMIM:Jaundice (in some)]
Jaundice (less common) [OMIM:Jaundice (less common)]
Jaundice (sometimes onset in the neonatal period) [OMIM:Jaundice (sometimes onset in the neonatal period)]
Hepatitis [MedDRA:10019717]
Inflammatory disease of liver (disorder) [Orphanet:29180]
Hepatitis [Orphanet:29180]
Quality:
Cross references:
Orphanet:29180 "Hepatitis/icterus/cholestasis" [Orphanet:29180]
OMIM: "Jaundice" [OMIM:Jaundice]
OMIM: "Icterus" [OMIM:Icterus]
OMIM: "Jaundice (1 patient)" [OMIM:Jaundice (1 patient)]
OMIM: "Jaundice (harderoporphyria)" [OMIM:Jaundice (harderoporphyria)]
OMIM: "Jaundice (in some patients)" [OMIM:Jaundice (in some patients)]
OMIM: "Jaundice (in some)" [OMIM:Jaundice (in some)]
OMIM: "Jaundice (less common)" [OMIM:Jaundice (less common)]
OMIM: "Jaundice (sometimes onset in the neonatal period)" [OMIM:Jaundice (sometimes onset in the neonatal period)]
UMLS:C0022346 "Jaundice" [HPO:0000952]
UMLS:C0022346 "Icterus" [Orphanet:29180]
UMLS:C0019158 "Hepatitis" [Orphanet:29180]
Is a (Direct Parents):
HPO         Cholestasis
MedDRA Haemolyses NEC
HPO         Dermatological manifestations of systemic disorders
Orphanet Decreased liver function
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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)
       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)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Haemolyses and related conditions(MedDRA:10018911)
       Haemolyses NEC(MedDRA:10018913)
          Jaundice(HPO:0000952)
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)
Ch├ędiak-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)