Hepatitis

Symptom Information:

Symptom ID: HPO:0012115
Synonyms:
Liver inflammation [HPO:0012115]
Hepatitis [OMIM:Hepatitis]
Hepatitis (rare) [OMIM:Hepatitis (rare)]
Hepatitis [MedDRA:10019717]
Inflammatory disease of liver (disorder) [Orphanet:29180]
Hepatitis [Orphanet:29180]
Hepatitis/icterus/cholestasis [Orphanet:29180]
Quality:
Cross references:
Orphanet:29180 "Hepatitis/icterus/cholestasis" [Orphanet:29180]
OMIM: "Hepatitis" [OMIM:Hepatitis]
OMIM: "Hepatitis (rare)" [OMIM:Hepatitis (rare)]
UMLS:C0019158 "Hepatitis" [Orphanet:29180]
Is a (Direct Parents):
Orphanet Jaundice
Orphanet Decreased liver function
HPO         Abnormality of the liver
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)
                Hepatitis(HPO:0012115)
MedDRA:
Database Frequency: 24 / 7739
Resource:

All diseases associated with this symptom:

Alström syndrome (Orphanet:64)
Argininosuccinic aciduria (Orphanet:23)
Autoimmune polyendocrinopathy type 2 (Orphanet:3143)
COMPLEMENT COMPONENT C1s DEFICIENCY (OMIM:613783)
CYANOSIS AND HEPATIC DISEASE (OMIM:219400)
Congenital bile acid synthesis defect type 3 (Orphanet:79302)
Dehydrated hereditary stomatocytosis (Orphanet:3202)
HALOTHANE HEPATITIS (OMIM:234350)
HEPATITIS B VACCINE, RESPONSE TO (OMIM:142395)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
Hyperornithinemia-hyperammonemia-homocitrullinuria (Orphanet:415)
Leprechaunism (Orphanet:508)
Lymphoid interstitial pneumonia (Orphanet:79128)
MERRF (Orphanet:551)
Menkes disease (Orphanet:565)
Neonatal hemochromatosis (Orphanet:446)
Niemann-Pick disease type C (Orphanet:646)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Renal cysts and diabetes syndrome (Orphanet:93111)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
TRICHOHEPATOENTERIC SYNDROME 2 (OMIM:614602)
Wolcott-Rallison syndrome (Orphanet:1667)
X-linked hyper-IgM syndrome (Orphanet:101088)
X-linked lymphoproliferative disease (Orphanet:2442)