Disease #05528 (MRD41 (mental retardation, autosomal dominant, type 41 (MRD-41)), OMIM:616944)

Official abbreviation	MRD41
Name	mental retardation, autosomal dominant, type 41 (MRD-41)
OMIM ID	616944
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TBL1XR1
Associated tissues	-
Disease features	autosomal dominant
Remarks	-
Date created	2018-12-02 17:44:54 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD