Hepatic fibrosis
Symptom Information:
Symptom ID: | HPO:0001395 | ||||||
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) MedDRA: Hepatobiliary disorders(MedDRA:10019805) Hepatic and hepatobiliary disorders(MedDRA:10019654) Hepatic fibrosis and cirrhosis(MedDRA:10019669) Hepatic fibrosis(HPO:0001395) |
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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) |