congenital myasthenic syndrome 2A

Summary

congenital myasthenic syndrome 2A is a rare disease^[1].

Key Facts

• congenital myasthenic syndrome 2A's instance of is recorded as rare disease^[2].
• congenital myasthenic syndrome 2A's instance of is recorded as class of disease^[3].
• congenital myasthenic syndrome 2A's subclass of is recorded as congenital myasthenic syndrome^[4].
• congenital myasthenic syndrome 2A's subclass of is recorded as postsynaptic congenital myasthenic syndrome^[5].
• congenital myasthenic syndrome 2A's subclass of is recorded as genetic disease^[6].
• congenital myasthenic syndrome 2A's subclass of is recorded as autosomal dominant disease^[7].
• congenital myasthenic syndrome 2A's OMIM ID is recorded as 616313^[8].
• congenital myasthenic syndrome 2A's OMIM ID is recorded as 616313^[9].
• congenital myasthenic syndrome 2A's Disease Ontology ID is recorded as DOID:0110681^[10].
• congenital myasthenic syndrome 2A's genetic association is recorded as CHRNB1^[11].
• congenital myasthenic syndrome 2A's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110681^[12].
• congenital myasthenic syndrome 2A's exact match is recorded as http://identifiers.org/doid/DOID:0110681^[13].
• congenital myasthenic syndrome 2A's UMLS CUI is recorded as C4225374^[14].
• congenital myasthenic syndrome 2A's GARD rare disease ID is recorded as 9895^[15].
• congenital myasthenic syndrome 2A's on focus list of Wikimedia project is recorded as WikiProject Medicine^[16].
• congenital myasthenic syndrome 2A's Mondo ID is recorded as MONDO_0014581^[17].
• congenital myasthenic syndrome 2A's UniProt disease ID is recorded as DI-04393^[18].