Disease #03299 (DFNB25 (deafness, autosomal recessive, type 25 (DFNB-25)), OMIM:613285)

Official abbreviation DFNB25
Name deafness, autosomal recessive, type 25 (DFNB-25)
OMIM ID 613285
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 5
Phenotype entries for this disease 1
Associated with 1 gene GRXCR1
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

5 entries on 1 page. Showing entries 1 - 5.
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00245701 - PubMed: Schraders 2010 - ? - - Pakistan - - - - DFNB25 - GRXCR1 GRXCR1 1 4 LOVD
00245703 - - - M - - Pakistani - - - - DFNB25 - GRXCR1 GRXCR1 1 2 LOVD
00245704 - - - F - - Dutch - - - - DFNB25 - GRXCR1 GRXCR1 1 1 LOVD
00245705 - - - F - - Dutch - - - - DFNB25 - GRXCR1 GRXCR1 1 3 LOVD
00428667 Fam5 PubMed: Wonkam 2022 3-generation family, 2 affected (1M,1F), unaffected carrier parents/relatives M no Ghana Africa - - - - DFNB25 - - GRXCR1 1 2 Yacouba Dia
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