Hepatitis
Symptom Information:
Symptom ID: | HPO:0012115 | |||||||
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) Hepatitis(HPO:0012115) MedDRA: |
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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) |