Disease #02352 (DFNA-11 (deafness, autosomal dominant, type 11 (DFNA-11)), OMIM:601317)

Official abbreviation DFNA-11
Name deafness, autosomal dominant, type 11 (DFNA-11)
OMIM ID 601317
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MYO7A
Associated tissues -
Disease features -
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00059026 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - no Israel Ashkenazi Jew - 0 - - DFNA-11 postlingual onset, ~5y, profound by age 12; also myopia - MYO7A 1 3 Zippi Brownstein
Legend   How to query