congenital myasthenic syndrome 13

Summary

congenital myasthenic syndrome 13 is a rare disease^[1].

Key Facts

• congenital myasthenic syndrome 13's instance of is recorded as rare disease^[2].
• congenital myasthenic syndrome 13's instance of is recorded as class of disease^[3].
• congenital myasthenic syndrome 13's subclass of is recorded as congenital myasthenic syndrome^[4].
• congenital myasthenic syndrome 13's subclass of is recorded as genetic disease^[5].
• congenital myasthenic syndrome 13's subclass of is recorded as autosomal recessive disease^[6].
• congenital myasthenic syndrome 13's OMIM ID is recorded as 614750^[7].
• congenital myasthenic syndrome 13's Disease Ontology ID is recorded as DOID:0110676^[8].
• congenital myasthenic syndrome 13's genetic association is recorded as DPAGT1^[9].
• congenital myasthenic syndrome 13's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110676^[10].
• congenital myasthenic syndrome 13's exact match is recorded as http://identifiers.org/doid/DOID:0110676^[11].
• congenital myasthenic syndrome 13's UMLS CUI is recorded as C3553645^[12].
• congenital myasthenic syndrome 13's on focus list of Wikimedia project is recorded as WikiProject Medicine^[13].
• congenital myasthenic syndrome 13's Mondo ID is recorded as MONDO_0013883^[14].
• congenital myasthenic syndrome 13's UniProt disease ID is recorded as DI-03511^[15].