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 Symptoms CheckerIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like KOHLSCHUTTER-TONZ SYNDROME; KTZS FAMILIAL ADENOMATOUS POLYPOSIS 3; FAP3 ESTROGEN RESISTANCE; ESTRR EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6; ARCI6 AUTOSOMAL RECESSIVE HYPOPHOSPHATEMIC RICKETS MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 3; MVA3