Hepatic fibrosis

Symptom Information:

Symptom ID: HPO:0001395
Synonyms:
Hepatic fibrosis [OMIM:Hepatic fibrosis]
Hepatic fibrosis (608002.0002) [OMIM:Hepatic fibrosis (608002.0002)]
Hepatic fibrosis (classic feature) [OMIM:Hepatic fibrosis (classic feature)]
Hepatic fibrosis (less common) [OMIM:Hepatic fibrosis (less common)]
Hepatic fibrosis [MedDRA:10019668]
Quality:
Cross references:
OMIM: "Hepatic fibrosis" [OMIM:Hepatic fibrosis]
OMIM: "Hepatic fibrosis (608002.0002)" [OMIM:Hepatic fibrosis (608002.0002)]
OMIM: "Hepatic fibrosis (classic feature)" [OMIM:Hepatic fibrosis (classic feature)]
OMIM: "Hepatic fibrosis (less common)" [OMIM:Hepatic fibrosis (less common)]
Is a (Direct Parents):
HPO         Abnormality of the liver
HPO         Hepatic bridging fibrosis
MedDRA Hepatic fibrosis and cirrhosis
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)
MedDRA:
Hepatobiliary disorders(MedDRA:10019805)
    Hepatic and hepatobiliary disorders(MedDRA:10019654)
       Hepatic fibrosis and cirrhosis(MedDRA:10019669)
          Hepatic fibrosis(HPO:0001395)
Database Frequency: 67 / 7739
Resource:

All diseases associated with this symptom:

ARIMA SYNDROME (OMIM:243910)
Acrocephalopolydactyly (Orphanet:221054)
Alström syndrome (Orphanet:64)
Argininemia (Orphanet:90)
Argininosuccinic aciduria (Orphanet:23)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 5 (OMIM:615983)
Cholesteryl ester storage disease (Orphanet:75234)
Citrullinemia type II (Orphanet:247585)
Cranioectodermal dysplasia (Orphanet:1515)
Cranioectodermal dysplasia 1 (OMIM:218330)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 (OMIM:224230)
EVC2 GENE (OMIM:607261)
Gaucher disease type 1 (Orphanet:77259)
Glycogen storage disease due to glycogen branching enzyme deficiency (Orphanet:367)
Glycogen storage disease due to glycogen debranching enzyme deficiency (Orphanet:366)
Hemochromatosis type 3 (Orphanet:225123)
Hemochromatosis type 4 (Orphanet:139491)
Hemochromatosis, type 1 (OMIM:235200)
Hemochromatosis, type 2A (OMIM:602390)
Hemochromatosis, type 2B (OMIM:613313)
Infantile regressive hypertriglyceridemia and hepatosteatosis (Orphanet:300293)
Jeune syndrome (Orphanet:474)
Joubert syndrome (Orphanet:475)
Joubert syndrome 1 (OMIM:213300)
Joubert syndrome 21 (OMIM:615636)
Joubert syndrome 28 (OMIM:617121)
Joubert syndrome 6 (OMIM:610688)
Joubert syndrome with hepatic defect (Orphanet:1454)
Joubert syndrome with oculorenal defect (Orphanet:2318)
Leigh syndrome (Orphanet:506)
Leprechaunism (Orphanet:508)
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate (Orphanet:314051)
Low phospholipid associated cholelithiasis (Orphanet:69663)
Lysosomal acid lipase deficiency (Orphanet:275761)
MEDNIK syndrome (Orphanet:171851)
MPI-CDG (Orphanet:79319)
Meckel syndrome, type 3 (OMIM:607361)
Meckel syndrome, type 6 (OMIM:612284)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET (OMIM:616263)
Neonatal diabetes - congenital hypothyroidism - congenital glaucoma - hepatic fibrosis - polycystic kidneys (Orphanet:79118)
Neonatal hemochromatosis (Orphanet:446)
Nephronophthisis 12 (OMIM:613820)
Nephronophthisis 16 (OMIM:615382)
Nephronophthisis 19 (OMIM:616217)
Nephronophthisis 3 (OMIM:604387)
Orofaciodigital syndrome type 1 (Orphanet:2750)
PMM2-CDG (Orphanet:79318)
PORPHYRIA CUTANEA TARDA, TYPE I (OMIM:176090)
Pearson syndrome (Orphanet:699)
Porphyria cutanea tarda (Orphanet:101330)
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
RENAL-HEPATIC-PANCREATIC DYSPLASIA 2 (OMIM:615415)
Renal-hepatic-pancreatic dysplasia (Orphanet:294415)
SPLENOPORTAL VASCULAR ANOMALIES (OMIM:271500)
Saldino-Mainzer syndrome (Orphanet:140969)
Senior-Boichis syndrome (Orphanet:84081)
Senior-Loken syndrome 3 (OMIM:606995)
Senior-Loken syndrome 9 (OMIM:616629)
Short rib-polydactyly syndrome, Majewski type (Orphanet:93269)
Short-rib thoracic dysplasia 1 with or without polydactyly (OMIM:208500)
Short-rib thoracic dysplasia 10 with or without polydactyly (OMIM:615630)
Syndromic diarrhea (Orphanet:84064)
Transaldolase deficiency (Orphanet:101028)
Wolman disease (Orphanet:75233)
Zellweger-like syndrome without peroxisomal anomalies (Orphanet:50812)