Disease #00836 (MRX-14 (mental retardation, X-linked, syndromic, type 14 (MRX-14)), OMIM:300676)

MyGenome LOVD - This database is for training purposes only

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

Official abbreviation	MRX-14
Name	mental retardation, X-linked, syndromic, type 14 (MRX-14)
OMIM ID	300676
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	UPF3B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A