neuropathy, hereditary motor and sensory, LOM type

Preferred Label : neuropathy, hereditary motor and sensory, LOM type;

MeSH synonym : hereditary motor and sensory neuropathy, LOM type; HMSNL; Charcot-Marie-Tooth disease, type 4D; HMSN4D; Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4d; Charcot-Marie-Tooth neuropathy, type 4d; CMT4D;

Details

Origin ID

C535716;

UMLS CUI

C1832334;

Currated CISMeF NLP mapping
- Charcot-Marie-Tooth disease type 4D [DO Concept]
- Charcot-Marie-Tooth disease type 4D [ORDO Disease]
- Charcot-Marie-Tooth disease type 4D (disorder) [SNOMED CT concept]
- Charcot-marie-tooth disease, demyelinating, type 4d [OMIM Phenotype]
MeSH term(s) associated for indexing
- charcot-marie-tooth disease [MeSH Descriptor]
- refsum disease [MeSH Descriptor]
ORDO relation(s)
- Charcot-Marie-Tooth disease type 4D [ORDO Disease]
Record concept(s)
- Neuropathy, hereditary motor and sensory, LOM type [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Charcot-Marie-Tooth disease type 4D [ORDO Disease]
- Charcot-Marie-Tooth disease type 4D [DO Concept]
- Charcot-Marie-Tooth disease type 4D (disorder) [SNOMED CT concept]
- Charcot-marie-tooth disease, demyelinating, type 4d [OMIM Phenotype]

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