Myopia 24, Autosomal Dominant (MYP24)

Alias:
Myp24
Myopia, Type 24, Autosomal Dominant
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Myopia 24, Autosomal Dominant, is also known as myp24. An important gene associated with Myopia 24, Autosomal Dominant is SLC39A5 (Solute Carrier Family 39 Member 5). Affiliated tissues include retina and eye, and related phenotype is high myopia.
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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1
8
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
Journal
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IF
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