Congenital hepatic fibrosis
Symptom Information:
Symptom ID: | HPO:0002612 | ||||||
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) Hepatic fibrosis(HPO:0001395) Congenital hepatic fibrosis(HPO:0002612) MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Hepatobiliary disorders congenital(MedDRA:10019806) Hepatobiliary abnormalities congenital(MedDRA:10019803) Congenital hepatic fibrosis(HPO:0002612) |
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Database Frequency: | 16 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Adams-Oliver syndrome | (Orphanet:974) |
Autosomal recessive polycystic kidney disease | (Orphanet:731) |
Cerebro-reno-digital syndrome | (Orphanet:1396) |
Cholesteryl ester storage disease | (Orphanet:75234) |
Congenital bile acid synthesis defect type 3 | (Orphanet:79302) |
DK1-CDG | (Orphanet:91131) |
Hemochromatosis type 2 | (Orphanet:79230) |
Hemochromatosis type 4 | (Orphanet:139491) |
Hepatic fibrosis - renal cysts - intellectual deficit | (Orphanet:2031) |
Joubert syndrome with hepatic defect | (Orphanet:1454) |
Laurence-Moon syndrome | (Orphanet:2377) |
MPI-CDG | (Orphanet:79319) |
Meckel syndrome | (Orphanet:564) |
Neonatal hemochromatosis | (Orphanet:446) |
Senior-Loken syndrome | (Orphanet:3156) |
Short rib-polydactyly syndrome, Verma-Naumoff type | (Orphanet:93271) |