Disease #00023 (DFNX4 (deafness, X-linked, type 4 (DFNX4)), OMIM:300066)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	DFNX4
Name	deafness, X-linked, type 4 (DFNX4)
OMIM ID	300066
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SMPX
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-07-30 11:33:04 +02:00 (CEST)
Date last edited	2021-05-18 08:59:44 +02:00 (CEST)

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