Disease #02624 (DFNB22 (deafness, autosomal recessive, type 2 (DFNB22)), OMIM:607039)

Official abbreviation DFNB22
Name deafness, autosomal recessive, type 2 (DFNB22)
OMIM ID 607039
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 OTOA
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-08-18 14:31:39 +02:00 (CEST)


Individuals

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00377583 P_OTOA - - F no Italy - - - - - DFNB22 - OTOA OTOA 1 1 Maria Pia Leone
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