Disease #00766 (MRX19 (mental retardation, X-linked, type 19 (MRX19)), OMIM:300844)

Official abbreviation MRX19
Name mental retardation, X-linked, type 19 (MRX19)
OMIM ID 300844
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene RPS6KA3
Associated tissues -
Disease features -
Remarks -