congenital myasthenic syndrome 11

Summary

congenital myasthenic syndrome 11 is a rare disease^[1].

Key Facts

• congenital myasthenic syndrome 11's instance of is recorded as rare disease^[2].
• congenital myasthenic syndrome 11's instance of is recorded as class of disease^[3].
• congenital myasthenic syndrome 11's subclass of is recorded as congenital myasthenic syndrome^[4].
• congenital myasthenic syndrome 11's subclass of is recorded as postsynaptic congenital myasthenic syndrome^[5].
• congenital myasthenic syndrome 11's subclass of is recorded as genetic disease^[6].
• congenital myasthenic syndrome 11's subclass of is recorded as autosomal recessive disease^[7].
• congenital myasthenic syndrome 11's MeSH descriptor ID is recorded as C563831^[8].
• congenital myasthenic syndrome 11's OMIM ID is recorded as 616326^[9].
• congenital myasthenic syndrome 11's Disease Ontology ID is recorded as DOID:0110675^[10].
• congenital myasthenic syndrome 11's NCI Thesaurus ID is recorded as C177546^[11].
• congenital myasthenic syndrome 11's genetic association is recorded as RAPSN^[12].
• congenital myasthenic syndrome 11's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110675^[13].
• congenital myasthenic syndrome 11's exact match is recorded as http://identifiers.org/doid/DOID:0110675^[14].
• congenital myasthenic syndrome 11's UMLS CUI is recorded as C1837094^[15].
• congenital myasthenic syndrome 11's on focus list of Wikimedia project is recorded as WikiProject Medicine^[16].
• congenital myasthenic syndrome 11's Mondo ID is recorded as MONDO_0014588^[17].
• congenital myasthenic syndrome 11's UniProt disease ID is recorded as DI-04401^[18].