Polycystic Liver Disease

Alias:
Congenital Polycystic Disease of Liver
Congenital Polycystic Liver Disease
Congenital Cystic Disease of Liver
Pld - [polycystic Liver Disease]
Congenital Cystic Liver Disease
Fibrocystic Liver Disease
Liver Disease, Polycystic
Polycystic Liver Disorder
Congenital Hepatic Cyst
Multiple Cysts of Liver
Polycystic Liver
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Polycystic Liver Disease, also known as congenital polycystic disease of liver, is related to polycystic liver disease 1 with or without kidney cysts and polycystic kidney disease 3 with or without polycystic liver disease, and has symptoms including hepatosplenomegaly An important gene associated with Polycystic Liver Disease is PRKCSH (Protein Kinase C Substrate 80K-H), and among its related pathways/superpathways are WNT Signaling and MicroRNAs in cardiomyocyte hypertrophy. The drugs Lanreotide and Octreotide have been mentioned in the context of this disorder. Affiliated tissues include liver and kidney, and related phenotypes are growth/size/body region and normal
Related ID:
MESH:C536330
ICD11:1361740083

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Adult
--
52
500
2

Medical Symptom

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Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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No data available

Related Drugs

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Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
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Publications
No data available

References Literature

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PMID
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IF
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