Disease #00021 (DFNX-1 (deafness, X-linked, type 1 (DFNX-1)), OMIM:304500)

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Official abbreviation	DFNX-1
Name	deafness, X-linked, type 1 (DFNX-1)
OMIM ID	304500
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PRPS1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-07-30 11:15:12 +02:00 (CEST)
Date last edited	N/A