Disease #06841 (MRXS11 (?Mental retardation, X-linked, syndromic 11, Shashi type), OMIM:300238)

Official abbreviation MRXS11
Name ?Mental retardation, X-linked, syndromic 11, Shashi type
OMIM ID 300238
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 RBMX
Associated tissues -
Disease features -
Remarks -