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Non-Syndromic X-Linked Intellectual Disability 104

Disease ID: disease_node_16355

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DbxrefMIM:300983
SubclassofDOID_0080012, DOID_0050776
Data SourceDOID
SynonymsMRX104, X-linked mental retardation 104
Doid Labelnon-syndromic X-linked intellectual disability 104
Doid DescriptionA non-syndromic X-linked intellectual disability characterized by global developmental delay, mild to severe intellectual disability with variable seizures, poor or absent speech, and behavioral problems in males that has_material_basis_in hemizygous mutation in the FRMPD4 gene on chromosome Xp22.2.
Has Material Basis InGENO_0000149
Disease Node Iddisease_node_16355
Doid IdDOID_0112018
LabelNon-Syndromic X-Linked Intellectual Disability 104