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Disease Ontology Browser
CK syndrome (DOID:0111898)
Alliance: disease page
Synonyms: X-linked intellectual disability-microcephaly-cortical malformation-thin habitus syndrome
Alt IDs: OMIM:300831, ORDO:251383, UMLS_CUI:C3151781
Definition: A lipid metabolism disorder characterized by increased methylsterol levels in cells and cerebrospinal fluid, mild to severe cognitive impairment, seizures, microcephaly, cerebral cortical malformations, dysmorphic facial features, and thin body habitus that has_material_basis_in hemizygous mutation in the NSDHL gene on chromosome Xq28.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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12/10/2024
MGI 6.24 		The Jackson Laboratory