hereditary type I motor and sensory neuropathy

Preferred Label : hereditary type I motor and sensory neuropathy;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0336505;

UMLS CUI

C0751036;

Automatic exact mappings (from CISMeF team)
- Charcot-marie-tooth disease, demyelinating, type 1b [OMIM Phenotype]
- Distal hereditary motor neuropathy type 1 [ORDO Disease]
Currated CISMeF NLP mapping
- Charcot Marie Tooth disease type 1 [Disease (Nov.)]
- Charcot-Marie-Tooth disease type 1 [DO Concept]
- Charcot-Marie-Tooth disease type 1 [ORDO Disease]
- Charcot-Marie-Tooth disease, type I (disorder) [SNOMED CT concept]
- Type I hereditary motor and sensory neuropathy [HPO term]
- charcot-marie-tooth disease, type i [SNOMED Notion]
Related record
- charcot-marie-tooth disease [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Charcot Marie Tooth disease type 1 [Disease (Nov.)]
- Charcot-Marie-Tooth disease type 1 [DO Concept]
- Charcot-Marie-Tooth disease type 1 [ORDO Disease]
- Charcot-Marie-Tooth disease, type I (disorder) [SNOMED CT concept]
- charcot-marie-tooth disease, type i [SNOMED Notion]