Polyneuropathy, lethal neonatal, axonal sensorimotor, autosomal recessive

Preferred Label : Polyneuropathy, lethal neonatal, axonal sensorimotor, autosomal recessive;

Type : Phenotype or locus, molecular basis unknown;

Prefixed ID : %604431;

Details

Origin ID

604431;

UMLS CUI

C1858353;

Automatic exact mappings (from CISMeF team)
- Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy [ORDO Disease]
Currated CISMeF NLP mapping
- Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) [SNOMED CT concept]
- polyneuropathy, lethal neonatal, axonal sensorimotor, autosomal recessive [MeSH concept]
- polyneuropathy, lethal neonatal, axonal sensorimotor, autosomal recessive [MeSH Supplementary Concept]
ORDO concept(s)
- Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) [SNOMED CT concept]
- polyneuropathy, lethal neonatal, axonal sensorimotor, autosomal recessive [MeSH Supplementary Concept]
- polyneuropathy, lethal neonatal, axonal sensorimotor, autosomal recessive [MeSH concept]

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