Disease #01130 (MRX-3 (mental retardation, X-linked, type 3 (MRX-3)), OMIM:309541)

MyGenome LOVD - This database is for training purposes only

LOVD v.3.0 Build 30 [ Current LOVD status ]
Log in

Official abbreviation	MRX-3
Name	mental retardation, X-linked, type 3 (MRX-3)
OMIM ID	309541
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	HCFC1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A