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syndromic X-linked intellectual disability Cabezas type (DOID:0060822)
Synonyms: Cabezas syndrome; syndromic X-linked mental retardation 15; mental retardation, X-linked, syndromic 15 (Cabezas type); MRSS; MRXS15; MRXSC; X-linked mental retardation with short stature; X-linked mental retardation with short stature, hypogonadism, and abnormal gait
Alt IDs: OMIM:300354, ICD10CM:Q87.8, ORDO:85293
Definition: A syndromic X-linked intellectual disability characterized by intellectual deficit, muscle wasting, short stature, hypogonadism, and bnormal 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 Xq23.


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/21/2017
MGI 6.08
The Jackson Laboratory