hereditary motor and sensory neuropathy, type IIC

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

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0565561;

UMLS CUI

C1853710;

Currated CISMeF NLP mapping
- Autosomal dominant Charcot-Marie-Tooth disease type 2C [ORDO Disease]
- Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder) [SNOMED CT concept]
- Charcot Marie Tooth disease type 2C [Disease (Nov.)]
- Charcot-Marie-Tooth disease axonal type 2C [DO Concept]
- Hereditary motor and sensory neuropathy, type iic [OMIM Phenotype]
Related record
- hereditary motor and sensory neuropathy, type IIC [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant Charcot-Marie-Tooth disease type 2C [ORDO Disease]
- Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder) [SNOMED CT concept]
- Hereditary motor and sensory neuropathy, type iic [OMIM Phenotype]