congenital myasthenic syndrome 4C
human disease
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congenital myasthenic syndrome 4C
Summary
congenital myasthenic syndrome 4C is a rare disease[1].
Key Facts
- congenital myasthenic syndrome 4C's instance of is recorded as rare disease[2].
- congenital myasthenic syndrome 4C's instance of is recorded as class of disease[3].
- congenital myasthenic syndrome 4C's subclass of is recorded as congenital myasthenic syndrome[4].
- congenital myasthenic syndrome 4C's subclass of is recorded as genetic disease[5].
- congenital myasthenic syndrome 4C's subclass of is recorded as autosomal recessive disease[6].
- congenital myasthenic syndrome 4C's OMIM ID is recorded as 608931[7].
- congenital myasthenic syndrome 4C's Disease Ontology ID is recorded as DOID:0110679[8].
- congenital myasthenic syndrome 4C's NCI Thesaurus ID is recorded as C174216[9].
- congenital myasthenic syndrome 4C's genetic association is recorded as CHRNE[10].
- congenital myasthenic syndrome 4C's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110679[11].
- congenital myasthenic syndrome 4C's exact match is recorded as http://identifiers.org/doid/DOID:0110679[12].
- congenital myasthenic syndrome 4C's UMLS CUI is recorded as C1837094[13].
- congenital myasthenic syndrome 4C's UMLS CUI is recorded as C1837092[14].
- congenital myasthenic syndrome 4C's UMLS CUI is recorded as C1837091[15].
- congenital myasthenic syndrome 4C's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- congenital myasthenic syndrome 4C's Mondo ID is recorded as MONDO_0012157[17].
- congenital myasthenic syndrome 4C's UniProt disease ID is recorded as DI-00369[18].