Disease #02908 (DFNB49 (deafness, autosomal recessive, type 49 (DFNB-49)), OMIM:610153)

Official abbreviation DFNB49
Name deafness, autosomal recessive, type 49 (DFNB-49)
OMIM ID 610153
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene MARVELD2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00428320 Fam18 PubMed: Wonkam 2022 5-generation family, 3 affected (2F, M) M yes Ghana Africa >12y - - - DFNB49 Post-lingual Non-syndromic hearing impairment, with variable age of onset with two family members with onset at 12 years of age and a third family member with onset at 8 years of age. MARVELD2 MARVELD2 1 3 Yacouba Dia
00428324 FamPat22 PubMed: Taghipour-Sheshdeh 2019 5-generation family, 3 affected (F, 2M), unaffected heterozygous carrier parents/relatives M yes Iran Arab - - - - DFNB49 see paper; ..., bilateral hearing loss (moderate to profound) - DFNB31, LHFPL5, MARVELD2, MYO15A, OTOF 5 3 Yacouba Dia
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