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Rpe65-Related Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy

Alias:
Rpe65-Related Lca/eosrd
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Rpe65-Related Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy, is also known as rpe65-related lca/eosrd. Affiliated tissues include eye.
Related ID：
MALACARDS：RP6003

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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43
RP6003

Medical Symptom

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Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Function
Score
Mutations
No data available

Related Drugs

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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
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