congenital myasthenic syndrome 8

Summary

congenital myasthenic syndrome 8 is a rare disease^[1].

Key Facts

• congenital myasthenic syndrome 8's instance of is recorded as rare disease^[2].
• congenital myasthenic syndrome 8's instance of is recorded as class of disease^[3].
• congenital myasthenic syndrome 8's subclass of is recorded as congenital myasthenic syndrome^[4].
• congenital myasthenic syndrome 8's subclass of is recorded as genetic disease^[5].
• congenital myasthenic syndrome 8's subclass of is recorded as autosomal recessive disease^[6].
• congenital myasthenic syndrome 8's OMIM ID is recorded as 615120^[7].
• congenital myasthenic syndrome 8's Disease Ontology ID is recorded as DOID:0110657^[8].
• congenital myasthenic syndrome 8's genetic association is recorded as AGRN^[9].
• congenital myasthenic syndrome 8's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110657^[10].
• congenital myasthenic syndrome 8's exact match is recorded as http://identifiers.org/doid/DOID:0110657^[11].
• congenital myasthenic syndrome 8's UMLS CUI is recorded as C3808739^[12].
• congenital myasthenic syndrome 8's on focus list of Wikimedia project is recorded as WikiProject Medicine^[13].
• congenital myasthenic syndrome 8's Mondo ID is recorded as MONDO_0014052^[14].
• congenital myasthenic syndrome 8's UniProt disease ID is recorded as DI-04109^[15].