Fish-Eye Disease (FED)

Alias:
Fed
Dyslipoproteinemic Corneal Dystrophy
Partial Lcat Deficiency
Alpha-Lcat Deficiency
Alpha-Lecithin:cholesterol Acyltransferase Deficiency
Lcata Deficiency
Lecithin Acyltransferase Deficiency
Disease, Fish-Eye
Fish Eye Disease
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Fish-Eye Disease, also known as fed, is related to lecithin:cholesterol acyltransferase deficiency and hypoalphalipoproteinemia, primary, 2. An important gene associated with Fish-Eye Disease is LCAT (Lecithin-Cholesterol Acyltransferase), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Plasma lipoprotein assembly, remodeling, and clearance. The drugs Hydrocortisone and Hydrocortisone acetate have been mentioned in the context of this disorder. Affiliated tissues include eye and heart, and related phenotypes are corneal opacity and decreased hdl cholesterol concentration
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Adolescent
<1/1000000
4
29
15

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
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