Retinal Dystrophy with Inner Retinal Dysfunction and Ganglion Cell Abnormalities (RDGCA)

Alias:
Retinal Dystrophy with Inner Retinal Dysfunction and Ganglion Cell Anomalies
Rdgca
Dystrophy, Retinal, with Inner Retinal Dysfunction and Ganglion Cell Abnormalities
Retinal Dystrophy with Inner Nuclear Layer and Ganglion Cell Anomalies
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Retinal Dystrophy with Inner Retinal Dysfunction and Ganglion Cell Abnormalities, is also known as retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies. An important gene associated with Retinal Dystrophy with Inner Retinal Dysfunction and Ganglion Cell Abnormalities is ITM2B (Integral Membrane Protein 2B). Affiliated tissues include eye and retina, and related phenotypes are photophobia and reduced visual acuity
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Adult
<1/1000000
1
5
1

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

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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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IF
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