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600970.1
Home
Subject Details
Country
United Arab Emirates
HPO Terms
Hearing impairment
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Sex
Unknown
Subject Variants
Variant Name
Allele Count
NM_153676.4:c.121G>A
1
NM_004999.4:c.3019C>T
1
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Remarks
Patient has heterozygous variants in MYO6 and USH1C. Both of these genes are hearing loss-associated.
References
Tlili et al. 2024
Related Subjects
Subject Id
Country
HPO Terms
Sex
Remarks
600970.2
United Arab Emirates
Hearing impairment
Unknown
Patient has heterozygous variants in MYO6 and LOXHD1. Both of these genes are hearing loss-associated.
Back to search Result
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العربية
About Us
News
Fellowships
العربية
Home
About Us
CTGA Database
CTGA Overview
Search Database
Submit to Database
Publications
Research Articles
Genetics Made Easy
Genetic Disorders in the Arab World
Reports
Conferences & Events
News
Gallery
Fellowships
Contact Us