Disease #02338 (DFNB9;AUNB1 (deafness, autosomal recessive, type 9), OMIM:601071)

Official abbreviation DFNB9;AUNB1
Name deafness, autosomal recessive, type 9
OMIM ID 601071
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 14
Phenotype entries for this disease 13
Associated with 1 gene OTOF
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2025-05-15 09:57:37 +02:00 (CEST)


Individuals

14 entries on 1 page. Showing entries 1 - 14.
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00059051 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - yes Israel Syria;Jewish - - - - DFNB9;AUNB1 congenital, profound HL, auditory neuropathy - OTOF 2 3 Zippi Brownstein
00249660 - - - - no - - - - - - DFNB9;AUNB1 auditory neuropathy - OTOF 2 1 Sophie Achard
00249661 - - - - - - - - - - - DFNB9;AUNB1 auditory neuropathy - OTOF 1 3 Sophie Achard
00249662 - - - - yes Mali - - - - - DFNB9;AUNB1 Auditory neuropathy profound deafness - OTOF 1 3 Sophie Achard
00249722 - - - M no France - - - - - DFNB9;AUNB1 - - OTOF 2 1 Sophie Achard
00249723 - - - M no (France) - - - - - DFNB9;AUNB1 auditory neuropathy - OTOF 2 1 Sophie Achard
00303507 - - sibling of 2 AUNB1 F no France - - - - - DFNB9;AUNB1 auditory neuropathy OTOF OTOF 2 2 Sophie Achard
00303509 - - - F no France - - - - - DFNB9;AUNB1 HP:0008504Moderate sensorineural hearing impairment temperature sensitive auditory neuropathy OTOF OTOF 2 1 Sophie Achard
00303510 - - - M no France - - - - - DFNB9;AUNB1 HP:0008527Congenital sensorineural hearing impairment profound deafness auditory neuropathy OTOF OTOF 2 1 Sophie Achard
00303513 - - - F no France - - - - - DFNB9;AUNB1 HP:0008527 Congenital sensorineural hearing impairment Profound deafness auditory neuropathy OTOF OTOF 2 1 Sophie Achard
00303514 - - - F ? - African - - - - DFNB9;AUNB1 HP:0008527Congenital sensorineural hearing impairment Auditory neuropathy OTOF OTOF 2 1 Sophie Achard
00303515 - - - M ? - African - - - - DFNB9;AUNB1 HP:0008527Congenital sensorineural hearing impairment Auditory neuropathy OTOF OTOF 2 1 Sophie Achard
00428415 Fam32 PubMed: Wonkam 2022 3-generation family, 2 affected sisters (2F), unaffected heterozygous carrier mother F no Ghana Africa - - - - DFNB9;AUNB1 - - OTOF 1 3 Yacouba Dia
00448502 - - - M yes Pakistan - - - - - DFNB9;AUNB1 - OTOF OTOF 1 1 Hina Khan
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