Cirrhosis, Familial
Table of contents:
Clinical Features
Top most frequent phenotypes and symptoms related to Cirrhosis, Familial
- Hypertension
- Fever
- Jaundice
- Abnormality of the liver
- Lethargy
- Cirrhosis
- Abdominal distention
- Pulmonary arterial hypertension
- Esophageal varix
- Micronodular cirrhosis
And another 2 symptoms. If you need more information about this disease we can help you.
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Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Cirrhosis, Familial Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
 KRT8.
By Fulgent Genetics Fulgent Genetics (United States).
KRT8
Specificity
100 %
Genes
50 % |
|
KRT18.
By Fulgent Genetics Fulgent Genetics (United States).
KRT18
Specificity
100 %
Genes
50 % |
You can get up to -6 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A; VDDR1A MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D METACARPAL 4-5 FUSION; MF4 CORNELIA DE LANGE SYNDROME 5; CDLS5 HAMAMY SYNDROME; HMMS CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 2 INTERMEDIATE NEMALINE MYOPATHY