proximal myotonic myopathy
human disease
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Summary
proximal myotonic myopathy is a rare disease[1].
Key Facts
- proximal myotonic myopathy's instance of is recorded as rare disease[2].
- proximal myotonic myopathy's instance of is recorded as class of disease[3].
- proximal myotonic myopathy's subclass of is recorded as myotonic disease[4].
- proximal myotonic myopathy's OMIM ID is recorded as 602668[5].
- proximal myotonic myopathy's Disease Ontology ID is recorded as DOID:0050759[6].
- proximal myotonic myopathy's Orphanet ID is recorded as 606[7].
- proximal myotonic myopathy's ICD-9-CM is recorded as 359.2[8].
- proximal myotonic myopathy's NCI Thesaurus ID is recorded as C84680[9].
- proximal myotonic myopathy's health specialty is recorded as neurology[10].
- proximal myotonic myopathy's genetic association is recorded as CNBP[11].
- proximal myotonic myopathy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050759[12].
- proximal myotonic myopathy's exact match is recorded as http://identifiers.org/doid/DOID:0050759[13].
- proximal myotonic myopathy's UMLS CUI is recorded as C2931689[14].
- proximal myotonic myopathy's ICD-10-CM is recorded as G71.19[15].
- proximal myotonic myopathy's ICD-10-CM is recorded as G71.1[16].
- proximal myotonic myopathy's GARD rare disease ID is recorded as 9728[17].
- proximal myotonic myopathy's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
- proximal myotonic myopathy's UniProt disease ID is recorded as DI-02024[19].