Hepatic calcification
Symptom Information:
Symptom ID: | HPO:0006559 | ||||||
Synonyms: |
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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) Hepatic calcification(HPO:0006559) Abnormality of the skeletal system(HPO:0000924) Ectopic calcification(HPO:0010766) Hepatic calcification(HPO:0006559) MedDRA: Hepatobiliary disorders(MedDRA:10019805) Hepatic and hepatobiliary disorders(MedDRA:10019654) Hepatic and hepatobiliary disorders NEC(MedDRA:10027681) Hepatic calcification(HPO:0006559) |
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Database Frequency: | 2 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Greenberg dysplasia | (Orphanet:1426) |