Disease #00445 (DFNA39 (deafness, autosomal dominant, type 39, with dentinogenesis (DFNA-39)), OMIM:605594)

Official abbreviation DFNA39
Name deafness, autosomal dominant, type 39, with dentinogenesis (DFNA-39)
OMIM ID 605594
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene DSPP
Associated tissues -
Disease features -
Remarks -
Date created 2014-07-09 12:59:49 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00019553 - - - - ? Korea, South (Republic) - - - - - DFNA39 - DSPP DSPP 1 1 Byung Yoon Choi
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