neurofibromatosis, familial spinal

Preferred Label : neurofibromatosis, familial spinal;

MeSH note : mutation in neurofibromin;

Origin ID

C563523;

UMLS CUI

C1834235;

Automatic exact mappings (from CISMeF team)
- neurofibromatosis 1 [DO Concept]
Currated CISMeF NLP mapping
- Familial spinal neurofibromatosis [ICD-11 More detail]
- Familial spinal neurofibromatosis [ORDO Disease]
- Familial spinal neurofibromatosis (disorder) [SNOMED CT concept]
- Neurofibromatosis, familial spinal [OMIM Phenotype]
MeSH term(s) associated for indexing
- neurofibromatoses [MeSH Descriptor]
Record concept(s)
- neurofibromatosis, familial spinal [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial spinal neurofibromatosis [ORDO Disease]
- Familial spinal neurofibromatosis [ICD-11 More detail]
- Familial spinal neurofibromatosis (disorder) [SNOMED CT concept]
- Neurofibromatosis, familial spinal [OMIM Phenotype]