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
605608.5.4
Home
Subject Details
Country
Syria
HPO Terms
Profound hearing impairment
Back to search Result
Sex
Male
Family History
Yes
Parental Consanguinity
Yes
Subject Variants
Variant Name
Allele Count
Associated Disease
NM_001146079.2:c.202C>T
2
Deafness, Autosomal Recessive 29
Download Table
Remarks
Brother of 605608.5.1
References
Tlili et al. 2024
Related Subjects
Subject Id
Country
HPO Terms
Sex
Family History
Parental Consanguinity
Remarks
605608.5.1
Syria
Profound hearing impairment
Male
Yes
Yes
605608.5.2
Syria
Profound hearing impairment
Male
Yes
Yes
Brother of 605608.5.1
605608.5.3
Syria
Profound hearing impairment
Male
Yes
Yes
Brother of 605608.5.1
605608.5.5
Syria
Male
Father of 605608.5.1
605608.5.6
Syria
Female
Mother of 605608.5.1
Back to search Result
© CAGS 2025. All rights reserved.
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