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Repository for lectin-assisted multimodality data
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CK syndrome
Summary
- Synonym
-
- X-linked intellectual disability-microcephaly-cortical malformation-thin habitus syndrome
- 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.
- Super Class
- X-linked recessive disease lipid metabolism disorder
External Links
- Disease Ontology
- DOID:0111898
- UMLS
- ORDO
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001263 | Global developmental delay |
| HP:0002126 | Polymicrogyria |
| HP:0100807 | Long fingers |
| HP:0000708 | Atypical behavior |
| HP:0000218 | High palate |
| HP:0001302 | Pachygyria |
| HP:0001382 | Joint hypermobility |
| HP:0000750 | Delayed speech and language development |
| HP:0001250 | Seizure |
| HP:0000358 | Posteriorly rotated ears |
