hyperCKmia

Summary

hyperCKmia is a rare disease^[1].

Key Facts

• hyperCKmia's instance of is recorded as rare disease^[2].
• hyperCKmia's instance of is recorded as class of disease^[3].
• hyperCKmia's subclass of is recorded as genetic disease^[4].
• hyperCKmia's subclass of is recorded as autosomal dominant disease^[5].
• hyperCKmia's subclass of is recorded as inherited metabolic disorder^[6].
• hyperCKmia's OMIM ID is recorded as 123320^[7].
• hyperCKmia's KEGG ID is recorded as H02181^[8].
• hyperCKmia's Disease Ontology ID is recorded as DOID:0111338^[9].
• hyperCKmia's medical examination is recorded as serum creatine kinase level^[10].
• hyperCKmia's has characteristic is recorded as abnormally high value^[11].
• hyperCKmia's NCI Thesaurus ID is recorded as C148327^[12].
• hyperCKmia's genetic association is recorded as CAV3^[13].
• hyperCKmia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111338^[14].
• hyperCKmia's exact match is recorded as http://identifiers.org/doid/DOID:0111338^[15].
• hyperCKmia's UMLS CUI is recorded as C0241005^[16].
• hyperCKmia's Mondo ID is recorded as MONDO_0007402^[17].
• hyperCKmia's UniProt disease ID is recorded as DI-01766^[18].