Charcot-Marie-Tooth disease, type 1D

Preferred Label : Charcot-Marie-Tooth disease, type 1D;

MeSH synonym : hereditary motor and sensory neuropathy 1D; HMSN 1D; Charcot-Marie-Tooth disease, demyelinating, type 1D; CMT1D; HMSN1D; HMSNID; Charcot-Marie-Tooth neuropathy, type 1D;

Détails

Origin ID

C537985;

UMLS CUI

C1843247;

Automatic exact mappings (from CISMeF team)
- Charcot-Marie-Tooth disease type 1D [ICD-11 More detail]
- EGR2 wt Allele [NCIt concept]
Currated CISMeF NLP mapping
- Charcot-Marie-Tooth disease type 1D [DO Concept]
- Charcot-Marie-Tooth disease type 1D [ORDO Disease]
- Charcot-Marie-Tooth disease type ID (disorder) [SNOMED CT concept]
- Charcot-marie-tooth disease, demyelinating, type 1d [OMIM Phenotype]
MeSH term(s) associated for indexing
- charcot-marie-tooth disease [MeSH Descriptor]
ORDO relation(s)
- Charcot-Marie-Tooth disease type 1D [ORDO Disease]
Record concept(s)
- Charcot-Marie-Tooth disease, Type 1D [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Charcot-Marie-Tooth disease type 1D [ORDO Disease]
- Charcot-Marie-Tooth disease type 1D [DO Concept]
- Charcot-Marie-Tooth disease type ID (disorder) [SNOMED CT concept]
- Charcot-marie-tooth disease, demyelinating, type 1d [OMIM Phenotype]

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