myasthenic syndromes, congenital

Preferred Label : myasthenic syndromes, congenital;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0328231;

UMLS CUI

C0751882;

Currated CISMeF NLP mapping
- Congenital Myasthenic Syndrome [NCIt concept]
- Congenital myasthenic syndrome [MedDRA Preferred Term]
- Congenital myasthenic syndrome [ORDO Disease]
- Congenital myasthenic syndrome (disorder) [SNOMED CT concept]
- Congenital myasthenic syndromes [ICD-11 Category]
- Myasthenic syndrome, congenital [OMIM phenotypic series]
- congenital myasthenic syndrome [Disease (Nov.)]
- congenital myasthenic syndrome [DO Concept]
MeSH narrower concept(s)
- congenital myasthenic syndromes, postsynaptic [MeSH concept]
- congenital myasthenic syndromes, presynaptic [MeSH concept]
- myasthenic syndromes, congenital, slow channel [MeSH concept]
Related record
- myasthenic syndromes, congenital [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Myasthenic Syndrome [NCIt concept]
- Congenital myasthenic syndrome [ORDO Disease]
- Congenital myasthenic syndrome [MedDRA Preferred Term]
- Congenital myasthenic syndrome (disorder) [SNOMED CT concept]
- congenital myasthenic syndrome [DO Concept]
- congenital myasthenic syndrome [Disease (Nov.)]