Congenital hepatic fibrosis

Symptom Information:

Symptom ID: HPO:0002612
Synonyms:
Congenital hepatic fibrosis (disorder) [Orphanet:28770]
Congenital hepatic fibrosis [Orphanet:28770]
Congenital hepatic fibrosis [MedDRA:10056533]
Hepatic fibrosis, congenital [OMIM:Hepatic fibrosis, congenital]
Quality:
Cross references:
Orphanet:28770 "Congenital hepatic fibrosis" [Orphanet:28770]
OMIM: "Hepatic fibrosis, congenital" [OMIM:Hepatic fibrosis, congenital]
UMLS:C0009714 "Congenital hepatic fibrosis" [Orphanet:28770]
Is a (Direct Parents):
HPO         Hepatic fibrosis
MedDRA Hepatobiliary abnormalities congenital
Orphanet Biliary tract abnormality
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)
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)