isolated elevated serum creatine phosphokinase levels

Summary
Synonym
  • elevated serum CPK
  • idiopathic hyperCKemia
  • isolated hyperCKemia
Definition
An inherited metabolic disorder characterized by elevated serum creatine kinase levels in the absence of muscle weakness or other symptoms that has_material_basis_in in some cases in heterozygous mutation in the CAV3 gene on chromosome 3p25.3.
Super Class
autosomal dominant disease inherited metabolic disorder
External Links
Disease Ontology
DOID:0111338
Mondo Disease Ontology
OMIM
Related Genes
Displaying entries 41 - 49 of 49 in total
Gene ID Gene Symbol Description Source
84197 POMK protein O-mannose kinase
84342 COG8 component of oligomeric golgi complex 8
84892 POMGNT2 protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)
84992 PIGY phosphatidylinositol glycan anchor biosynthesis class Y
85365 ALG2 ALG2 alpha-1,3/1,6-mannosyltransferase
91949 COG7 component of oligomeric golgi complex 7
148789 B3GALNT2 beta-1,3-N-acetylgalactosaminyltransferase 2
199857 ALG14 ALG14 UDP-N-acetylglucosaminyltransferase subunit
729920 CRPPA CDP-L-ribitol pyrophosphorylase A

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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