Disease #02462 (DFNB21 (deafness, autosomal recessive, type 21 (DFNB-21)), OMIM:603629)

Official abbreviation DFNB21
Name deafness, autosomal recessive, type 21 (DFNB-21)
OMIM ID 603629
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 TECTA
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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00080843 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - DFNB21 Deafness, autosomal recessive 21 (OMIM:603629) TECTA TECTA 1 1 Daniel Trujillano
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