Disease #03798 (DFNB18B (deafness, autosomal recessive, type 18b (DFNB-18B)), OMIM:614945)

Official abbreviation DFNB18B
Name deafness, autosomal recessive, type 18b (DFNB-18B)
OMIM ID 614945
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene OTOG
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-01-28 14:25:06 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00154485 - - - M yes Israel - - - - - DFNB18B - - OTOG 1 1 Nada Danial-Farran
00428674 Fam33 PubMed: Wonkam 2022 3-generation family, 2 affected (1M,1F) F no Ghana Africa - - - - DFNB18B - - OTOG 2 2 Yacouba Dia
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