Disease #02207 (MRX99 (mental retardation, X-linked, type 99 (MRX99)), OMIM:300919)

Official abbreviation MRX99
Name mental retardation, X-linked, type 99 (MRX99)
OMIM ID 300919
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene USP9X
Associated tissues -
Disease features -
Remarks -

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