hyperCKmia
human disease
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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 is a type of genetic disease[4].
- hyperCKmia is a type of autosomal dominant disease[5].
- hyperCKmia is a type of inherited metabolic disorder[6].
- hyperCKmia's medical examination is recorded as serum creatine kinase level[7].
- hyperCKmia's has characteristic is recorded as abnormally high value[8].
- hyperCKmia's NCI Thesaurus ID is recorded as C148327[9].
- hyperCKmia's genetic association is recorded as CAV3[10].
- hyperCKmia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111338[11].
- hyperCKmia's exact match is recorded as http://identifiers.org/doid/DOID:0111338[12].