Congenital and developmental myasthenia

Preferred Label : Congenital and developmental myasthenia;

Diag associé à un acte (%) : 64.8;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

G702;

UMLS CUI

C0451670;

Automatic exact mappings (from CISMeF team)
- Congenital and developmental myasthenia (disorder) [SNOMED CT concept]
- Congenital myasthenic syndromes [ICD-11 Category]
Metaterm(s)
- allergy and immunology [CISMeF Metaterm]
- neonatology [CISMeF Metaterm]
Orphanet concepts
- Congenital myasthenic syndrome [ORDO Disease]
- Congenital myasthenic syndromes with glycosylation defect [ORDO Disease]
- Genetic neuromuscular junction disease [ORDO Disease]
- Neuromuscular junction disease [ORDO Disease]
- Postsynaptic congenital myasthenic syndromes [ORDO Disease]
- Presynaptic congenital myasthenic syndromes [ORDO Disease]
- Synaptic congenital myasthenic syndromes [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital and developmental myasthenia (disorder) [SNOMED CT concept]
- Congenital myasthenic syndromes [ICD-11 Category]

Keyword's position in hierarchy(ies) :

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