congenital myasthenic syndrome 5

Summary

congenital myasthenic syndrome 5 is a rare disease^[1].

Key Facts

• congenital myasthenic syndrome 5's instance of is recorded as rare disease^[2].
• congenital myasthenic syndrome 5's instance of is recorded as class of disease^[3].
• congenital myasthenic syndrome 5's subclass of is recorded as congenital myasthenic syndrome^[4].
• congenital myasthenic syndrome 5's subclass of is recorded as genetic disease^[5].
• congenital myasthenic syndrome 5's subclass of is recorded as autosomal recessive disease^[6].
• congenital myasthenic syndrome 5's OMIM ID is recorded as 603034^[7].
• congenital myasthenic syndrome 5's Disease Ontology ID is recorded as DOID:0110667^[8].
• congenital myasthenic syndrome 5's Orphanet ID is recorded as 98915^[9].
• congenital myasthenic syndrome 5's NCI Thesaurus ID is recorded as C129304^[10].
• congenital myasthenic syndrome 5's genetic association is recorded as COLQ^[11].
• congenital myasthenic syndrome 5's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110667^[12].
• congenital myasthenic syndrome 5's exact match is recorded as http://identifiers.org/doid/DOID:0110667^[13].
• congenital myasthenic syndrome 5's UMLS CUI is recorded as C5681640^[14].
• congenital myasthenic syndrome 5's ICD-10-CM is recorded as G70.2^[15].
• congenital myasthenic syndrome 5's on focus list of Wikimedia project is recorded as WikiProject Medicine^[16].
• congenital myasthenic syndrome 5's Mondo ID is recorded as MONDO_0020346^[17].
• congenital myasthenic syndrome 5's UniProt disease ID is recorded as DI-00366^[18].