Disease #02338

Official abbreviation DFNB-9
Name deafness, autosomal recessive, type 9 (DFNB-9)
OMIM ID 601071
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 6
Phenotype entries for this disease 5
Associated with 1 gene OTOF
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Disease features -
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Individuals

6 entries on 1 page. Showing entries 1 - 6.
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00059051 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - yes Israel Syrian Jews - 0 - - DFNB-9 congenital, profound HL, auditory neuropathy - OTOF 2 3 Zippi Brownstein
00249660 - - - - no - - - 0 - - DFNB-9 auditory neuropathy - OTOF 2 1 Sophie Achard
00249661 - - - - - - - - 0 - - DFNB-9 auditory neuropathy - OTOF 1 3 Sophie Achard
00249662 - - - - yes Mali - - 0 - - DFNB-9 Auditory neuropathy profound deafness - OTOF 1 3 Sophie Achard
00249722 - - - M no France - - 0 - - DFNB-9 - - OTOF 2 1 Sophie Achard
00249723 - - - M no (France) - - 0 - - DFNB-9 auditory neuropathy - OTOF 2 1 Sophie Achard
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