congenital myasthenic syndrome 3B

Summary

congenital myasthenic syndrome 3B is a rare disease^[1].

Key Facts

• congenital myasthenic syndrome 3B's instance of is recorded as rare disease^[2].
• congenital myasthenic syndrome 3B's instance of is recorded as class of disease^[3].
• congenital myasthenic syndrome 3B's subclass of is recorded as congenital myasthenic syndrome^[4].
• congenital myasthenic syndrome 3B's subclass of is recorded as postsynaptic congenital myasthenic syndrome^[5].
• congenital myasthenic syndrome 3B's subclass of is recorded as genetic disease^[6].
• congenital myasthenic syndrome 3B's OMIM ID is recorded as 616322^[7].
• congenital myasthenic syndrome 3B's Disease Ontology ID is recorded as DOID:0110665^[8].
• congenital myasthenic syndrome 3B's genetic association is recorded as CHRND^[9].
• congenital myasthenic syndrome 3B's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110665^[10].
• congenital myasthenic syndrome 3B's exact match is recorded as http://identifiers.org/doid/DOID:0110665^[11].
• congenital myasthenic syndrome 3B's UMLS CUI is recorded as C4225371^[12].
• congenital myasthenic syndrome 3B's on focus list of Wikimedia project is recorded as WikiProject Medicine^[13].
• congenital myasthenic syndrome 3B's Mondo ID is recorded as MONDO_0014584^[14].
• congenital myasthenic syndrome 3B's UniProt disease ID is recorded as DI-04395^[15].