Abnormality of the liver
Symptom Information:
Symptom ID: | HPO:0001392 | ||||||
Synonyms: |
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Quality: | |||||||
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) MedDRA: |
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Database Frequency: | 28 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 13 | (OMIM:615990) |
Bardet-Biedl syndrome 6 | (OMIM:605231) |
Blue rubber bleb nevus | (Orphanet:1059) |
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
Congenital atransferrinemia | (Orphanet:1195) |
Fetal Gaucher disease | (Orphanet:85212) |
GM1 gangliosidosis type 2 | (Orphanet:79256) |
HYPERVITAMINOSIS A, SUSCEPTIBILITY TO | (OMIM:240150) |
Hepatic veno-occlusive disease - immunodeficiency | (Orphanet:79124) |
Leprechaunism | (Orphanet:508) |
MELAS | (Orphanet:550) |
MERRF | (Orphanet:551) |
Mediterranean macrothrombocytopenia | (Orphanet:101022) |
Menkes disease | (Orphanet:565) |
Microcytic anemia with liver iron overload | (Orphanet:83642) |
Mitochondrial trifunctional protein deficiency | (Orphanet:746) |
Nephronophthisis 2 | (OMIM:602088) |
Nephronophthisis 3 | (OMIM:604387) |
Nephronophthisis 9 | (OMIM:613824) |
Nephronophthisis-like nephropathy 1 | (OMIM:613159) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 4 | (OMIM:610131) |
Retroperitoneal fibrosis | (Orphanet:49041) |
Tyrosinemia type 3 | (Orphanet:69723) |
Von Hippel-Lindau disease | (Orphanet:892) |
Wilson disease | (Orphanet:905) |