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CK syndrome
Disease Summary
Associated Targets (1)
Tbio
1
Uniprot Description A disorder characterized by mild to severe cognitive impairment, seizures, microcephaly, cerebral cortical malformations, dysmorphic facial features, and thin body habitus.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
OMIM:300831
Orphanet:251383
UMLS:C3151781
MONDO:0010441
High level summary of knowledge for a disease, including descriptions and datasource references.