keratoderma palmoplantar spastic paralysis

Preferred Label : keratoderma palmoplantar spastic paralysis;

MeSH synonym : keratoderma, palmoplantar, with nail dystrophy and hereditary motor-sensory neuropathy; axonal neuropathy with palmoplantar keratoderma; Charcot-Marie-Tooth disease with palmoplantar keratoderma and nail dystrophy;

Details

Origin ID

C536153;

UMLS CUI

C1835671;

Currated CISMeF NLP mapping
- Keratoderma, palmoplantar, with nail dystrophy and hereditary motor-sensory neuropathy [OMIM Phenotype]
- Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome (disorder) [SNOMED CT concept]
- Palmoplantar keratoderma, spastic paralysis syndrome (disorder) [SNOMED CT concept]
- Palmoplantar keratoderma-spastic paralysis syndrome [ORDO Disease]
MeSH term(s) associated for indexing
- charcot-marie-tooth disease [MeSH Descriptor]
- keratoderma, palmoplantar [MeSH Descriptor]
- nail diseases [MeSH Descriptor]
ORDO relation(s)
- Palmoplantar keratoderma-spastic paralysis syndrome [ORDO Disease]
Record concept(s)
- Keratoderma palmoplantar spastic paralysis [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Keratoderma, palmoplantar, with nail dystrophy and hereditary motor-sensory neuropathy [OMIM Phenotype]
- Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome (disorder) [SNOMED CT concept]

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