neuropathy, hereditary motor and sensory, okinawa type

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

MeSH synonym : HMSNP; HEREDITARY MOTOR AND SENSORY NEUROPATHY, PROXIMAL TYPE; HMSNO;

Details

Origin ID

C535717;

UMLS CUI

C1858338;

CISMeF manual mappings
- Hereditary motor and sensory neuropathy Okinawa type (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Autosomal dominant Charcot-Marie-Tooth disease type 2 [ORDO Disease]
- Charcot Marie Tooth disease type 2 [Disease (Nov.)]
- Charcot-Marie-Tooth disease type 2 [DO Concept]
- Charcot-Marie-Tooth disease, type II (disorder) [SNOMED CT concept]
- Hereditary motor and sensory neuropathy, Okinawa type [ORDO Disease]
- Hereditary motor or sensory neuropathy, Okinawa type [ICD-11 More detail]
- Neuropathy, hereditary motor and sensory, okinawa type [OMIM Phenotype]
- dominant hereditary sensory neuropathy, type ii [SNOMED Notion]
Has phenotype(s) (HPO)
- Muscle weakness and atrophy [HPO term]
MeSH term(s) associated for indexing
- hereditary sensory and motor neuropathy [MeSH Descriptor]
ORDO relation(s)
- Hereditary motor and sensory neuropathy, Okinawa type [ORDO Disease]
Record concept(s)
- Neuropathy, hereditary motor and sensory, Okinawa type [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary motor and sensory neuropathy Okinawa type (disorder) [SNOMED CT concept]
- Hereditary motor and sensory neuropathy, Okinawa type [ORDO Disease]
- Neuropathy, hereditary motor and sensory, okinawa type [OMIM Phenotype]

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