Disease #02338

Official abbreviation DFNB-9
Name deafness, autosomal recessive, type 9 (DFNB-9)
OMIM ID 601071
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene OTOF
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Individuals

1 entry on 1 page. Showing entry 1.
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00059051 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - yes Israel Syrian Jews - 0 - - DFNB-9 congenital, profound HL, auditory neuropathy - OTOF 2 3 Zippi Brownstein
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