metabolic myopathy due to lactate transporter defect
human disease
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metabolic myopathy due to lactate transporter defect
Summary
metabolic myopathy due to lactate transporter defect is a class of disease[1].
Key Facts
- metabolic myopathy due to lactate transporter defect's instance of is recorded as class of disease[2].
- metabolic myopathy due to lactate transporter defect's subclass of is recorded as metabolic myopathy[3].
- metabolic myopathy due to lactate transporter defect's MeSH descriptor ID is recorded as C565449[4].
- metabolic myopathy due to lactate transporter defect's OMIM ID is recorded as 245340[5].
- metabolic myopathy due to lactate transporter defect's KEGG ID is recorded as H01248[6].
- metabolic myopathy due to lactate transporter defect's Orphanet ID is recorded as 171690[7].
- metabolic myopathy due to lactate transporter defect's genetic association is recorded as SLC16A1[8].
- metabolic myopathy due to lactate transporter defect's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_171690[9].
- metabolic myopathy due to lactate transporter defect's UMLS CUI is recorded as C1855577[10].
- metabolic myopathy due to lactate transporter defect's ICD-10-CM is recorded as G72.8[11].
- metabolic myopathy due to lactate transporter defect's Mondo ID is recorded as MONDO_0009501[12].
- metabolic myopathy due to lactate transporter defect's UniProt disease ID is recorded as DI-02351[13].