Disease #00294

Official abbreviation DFNB-86
Name deafness, nonsyndromic, autosomal recessive, type 86 (DFNB-86)
OMIM ID 614617
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 4
Phenotype entries for this disease 1
Associated with 1 gene TBC1D24
Associated tissues -
Disease features -
Remarks -


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00004158 - PubMed: Rehman et al., 2014 - F yes Pakistan - - 0 - - DFNB-86 - TBC1D24 TBC1D24 1 1 Philippe Campeau
00004159 - PubMed: Rehman et al., 2014 - M yes Pakistan - - 0 - - DFNB-86 - TBC1D24 TBC1D24 1 1 Philippe Campeau
00059050 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - no Israel Arab - 0 - - DFNB-86 - - TBC1D24 1 3 Zippi Brownstein
00163777 - - - M yes - - - 0 - - DFNB-86 - - TBC1D24 1 1 Nada Danial-Farran
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