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Retinitis Pigmentosa 35 (RP35)

Alias:
Rp35
Retinitis Pigmentosa, Type 35
Retinitis Pigmentosa-35
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Retinitis Pigmentosa 35, also known as rp35, is related to cone-rod dystrophy 10 and meninges sarcoma. An important gene associated with Retinitis Pigmentosa 35 is SEMA4A (Semaphorin 4A). Affiliated tissues include retina and eye, and related phenotypes are blindness and reduced visual acuity
Related ID：
MALACARDS：RTN064
OMIM：610282
MESH：C565206

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
6
34
4
RTN064

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

Title
PMID
Journal
Year
IF
No Data Found!
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