Disease #06849 (MRXS99F (Mental retardation, X-linked 99, syndromic, female-restricted), OMIM:300968)

Official abbreviation MRXS99F
Name Mental retardation, X-linked 99, syndromic, female-restricted
OMIM ID 300968
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 USP9X
Associated tissues -
Disease features -
Remarks -

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