Disease #03244

Official abbreviation DFNB-77
Name deafness, autosomal recessive, type 77 (DFNB-77)
OMIM ID 613079
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene LOXHD1
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Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00059048 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - yes Israel Arab - 0 - - DFNB-77 congenital, profound HL - LOXHD1 1 2 Zippi Brownstein
00059049 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - no Israel AJ - 0 - - DFNB-77 congenital, profound NSHL - LOXHD1 2 2 Zippi Brownstein
00163776 - - - M - - Middle Eastern - 0 - - DFNB-77 - - LOXHD1 1 1 Nada Danial-Farran
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