Disease #02858 (DFNB23 (deafness, autosomal recessive, type 23 (DFNB-23)), OMIM:609533)

Official abbreviation DFNB23
Name deafness, autosomal recessive, type 23 (DFNB-23)
OMIM ID 609533
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 PCDH15
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

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00081034 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - DFNB23 Deafness, autosomal recessive 23 (OMIM:609533) PCDH15 PCDH15 1 1 Daniel Trujillano
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