Disease #00017 (MRXS-10 (mental retardation, X-linked syndromic, type 10 (MRXS-10)), OMIM:300220)

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Official abbreviation	MRXS-10
Name	mental retardation, X-linked syndromic, type 10 (MRXS-10)
OMIM ID	300220
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	HSD17B10
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-07-23 10:48:25 +02:00 (CEST)
Date last edited	N/A