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Syndromic X-Linked Intellectual Disability Cabezas Type

Disease ID: disease_node_19240

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DbxrefGARD:13244, ICD10CM:Q87.8, MIM:300354, ORDO:85293
SubclassofDOID_0060309
Data SourceDOID
SynonymsCabezas syndrome, syndromic X-linked mental retardation 15, MRSS, MRXS15, MRXSC, X-linked mental retardation with short stature, X-linked mental retardation with short stature, hypogonadism, and abnormal gait, mental retardation, X-linked, syndromic 15, mental retardation, X-linked, syndromic 15 (Cabezas type)
Doid Labelsyndromic X-linked intellectual disability Cabezas type
Doid DescriptionA syndromic X-linked intellectual disability characterized by intellectual deficit, muscle wasting, short stature, hypogonadism, and abnormal gait, with variable occurrence of prominent lower lip, kyphosis, joint hyperextensibility, tremor, decreased fine motor coordination and impaired speech that has_material_basis_in mutation in the CUL4B gene on chromosome Xq24.
Disease Node Iddisease_node_19240
Doid IdDOID_0060822
LabelSyndromic X-Linked Intellectual Disability Cabezas Type