Disease #03486 (DFNB89 (deafness, autosomal recessive, type 89 (DFNB89)), OMIM:613916)

Official abbreviation DFNB89
Name deafness, autosomal recessive, type 89 (DFNB89)
OMIM ID 613916
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene KARS
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-03-23 10:08:35 +01:00 (CET)


Individuals

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00428668 Fam19 PubMed: Wonkam 2022 3-generation family, 2 affected (1M,1F), unaffected carrier mother F no Ghana Africa - - - - DFNB89 - - KARS 1 2 Yacouba Dia
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