Spinal arachnoiditis

Preferred Label : Spinal arachnoiditis;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant;

Prefixed ID : %182950;

Details

Origin ID

182950;

UMLS CUI

C1710146;

Automatic exact mappings (from CISMeF team)
- Arachnoiditis [ORDO Disease]
- Spinal arachnoid [ICD-11 Extension code]
- Spinal arachnoid [ICHI extension code]
- Spinal arachnoiditis [ICD-11 More detail]
- Structure of spinal arachnoid (body structure) [SNOMED CT concept]
- spinal arachnoid [SNOMED Notion]
Currated CISMeF NLP mapping
- Spinal Arachnoiditis [NCIt concept]
- Spinal arachnoiditis [MedDRA LLT]
- Spinal arachnoiditis (disorder) [SNOMED CT concept]
- familial spinal arachnoiditis [MeSH concept]
- familial spinal arachnoiditis [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of metabolism/homeostasis [HPO term]
- Abnormality of the skeletal system [HPO term]
- Autosomal dominant inheritance [HPO term]
- Spastic paraparesis [HPO term]
ORDO concept(s)
- Arachnoiditis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spinal Arachnoiditis [NCIt concept]
- Spinal arachnoiditis [MedDRA LLT]
- Spinal arachnoiditis (disorder) [SNOMED CT concept]
- familial spinal arachnoiditis [MeSH Supplementary Concept]
- familial spinal arachnoiditis [MeSH concept]

Keyword's position in hierarchy(ies) :

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