neutral lipid storage myopathy
human disease
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neutral lipid storage myopathy
Summary
neutral lipid storage myopathy is a rare disease[1].
Key Facts
- neutral lipid storage myopathy's instance of is recorded as rare disease[2].
- neutral lipid storage myopathy's instance of is recorded as class of disease[3].
- neutral lipid storage myopathy's subclass of is recorded as neutral lipid storage disease[4].
- neutral lipid storage myopathy's OMIM ID is recorded as 610717[5].
- neutral lipid storage myopathy's KEGG ID is recorded as H01297[6].
- neutral lipid storage myopathy's Orphanet ID is recorded as 98908[7].
- neutral lipid storage myopathy's genetic association is recorded as PNPLA2[8].
- neutral lipid storage myopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_98908[9].
- neutral lipid storage myopathy's UMLS CUI is recorded as C1853136[10].
- neutral lipid storage myopathy's ICD-10-CM is recorded as E75.5[11].
- neutral lipid storage myopathy's GARD rare disease ID is recorded as 10288[12].
- neutral lipid storage myopathy's Mondo ID is recorded as MONDO_0012545[13].
- neutral lipid storage myopathy's Genetics Home Reference Conditions ID is recorded as neutral-lipid-storage-disease-with-myopathy[14].
- neutral lipid storage myopathy's UniProt disease ID is recorded as DI-02050[15].