Disease #01130 (MRX3 (mental retardation, X-linked, type 3 (MRX3)), OMIM:309541)

Official abbreviation MRX3
Name mental retardation, X-linked, type 3 (MRX3)
OMIM ID 309541
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene HCFC1
Associated tissues -
Disease features -
Remarks -

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