Compton-North congenital myopathy
Human disease
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Compton-North congenital myopathy
Summary
Compton-North congenital myopathy is a rare disease[1].
Key Facts
- Compton-North congenital myopathy's instance of is recorded as rare disease[2].
- Compton-North congenital myopathy's instance of is recorded as class of disease[3].
- Compton-North congenital myopathy's subclass of is recorded as congenital myopathy[4].
- Compton-North congenital myopathy's MeSH descriptor ID is recorded as C567261[5].
- Compton-North congenital myopathy's OMIM ID is recorded as 612540[6].
- Compton-North congenital myopathy's Disease Ontology ID is recorded as DOID:0080101[7].
- Compton-North congenital myopathy's Orphanet ID is recorded as 210163[8].
- Compton-North congenital myopathy's genetic association is recorded as CNTN1[9].
- Compton-North congenital myopathy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080101[10].
- Compton-North congenital myopathy's exact match is recorded as http://identifiers.org/doid/DOID:0080101[11].
- Compton-North congenital myopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_210163[12].
- Compton-North congenital myopathy's UMLS CUI is recorded as C2675527[13].
- Compton-North congenital myopathy's UMLS CUI is recorded as C4750773[14].
- Compton-North congenital myopathy's ICD-10-CM is recorded as G71.2[15].
- Compton-North congenital myopathy's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- Compton-North congenital myopathy's Mondo ID is recorded as MONDO_0012929[17].
- Compton-North congenital myopathy's UniProt disease ID is recorded as DI-01385[18].