Usher Syndrome Type 2 (USH2)

Alias:
Ush2
Usher Syndrome, Type Ii
Usher Syndrome Type Ii
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Usher Syndrome Type 2, also known as ush2, is related to usher syndrome, type iic and usher syndrome, type iid. An important gene associated with Usher Syndrome Type 2 is USH2A (Usherin), and among its related pathways/superpathways are Olfactory Signaling Pathway and Ciliary landscape. Affiliated tissues include eye and retina, and related phenotypes are sensorineural hearing impairment and abnormal electroretinogram
Related ID:
MESH:D052245

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Newborn
1-9/100000
63
584
78

Medical Symptom

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

Gene & Mutation

#
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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