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
Mondo Disease Ontology
UMLS
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
50814 NSDHL NAD(P) dependent steroid dehydrogenase-like
The Human Phenotype Ontology
Displaying entries 11 - 20 of 42 in total
HPO ID HPO Term
HP:0000286 Epicanthus
HP:0002938 Lumbar hyperlordosis
HP:0000718 Aggressive behavior
HP:0100807 Long fingers
HP:0001249 Intellectual disability
HP:0000486 Strabismus
HP:0002360 Sleep abnormality
HP:0000218 High palate
HP:0001250 Seizure
HP:0000272 Malar flattening
Displaying 1 entry
Gene ID Gene Symbol Description
50814 NSDHL NAD(P) dependent steroid dehydrogenase-like

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024