Intervertebral disc disease

Preferred Label : Intervertebral disc disease;

Symbol : IDD;

CISMeF acronym : IDD; LDD;

Type : Phenotype, molecular basis known;

Included titles and symbols : Lumbar disc disease; Lumbar disc herniation, susceptibility to; Lumbar disc degeneration, susceptibility to; LDD;

Description : Lumbar disc disease is caused by degeneration of intervertebral discs of the lumbar spine. One of the most common musculoskeletal disorders, it has strong genetic determinants (Matsui et al., 1998; Battie et al., 1995; Sambrook et al., 1999).;

Prefixed ID : #603932;

Details

Origin ID

603932;

UMLS CUI

C0158252;

Automatic exact mappings (from CISMeF team)
- DiGeorge syndrome critical region gene 2 [HGNC gene]
- Dysplastic gangliocytoma of the cerebellum [HPO term]
- Lhermitte-Duclos disease [ORDO Disease]
- Lumbar disc disease [MedDRA LLT]
- Relative density (property) (qualifier value) [SNOMED CT concept]
- collagen type IX alpha 3 chain [ORDO Gene]
- collagen type IX alpha 3 chain [HGNC gene]
- lumbar disc disease [MeSH concept]
Currated CISMeF NLP mapping
- Intervertebral disc disease [MeSH concept]
- intervertebral disc disease [MeSH Supplementary Concept]
- intervertebral disc disorder [Disease (Nov.)]
Genes related to phenotype
- Asporin [OMIM gene]
- Cartilage intermediate layer protein [OMIM gene]
- Collagen, type XI, alpha-1 [OMIM gene]
- Collagen, type ix, alpha-3 [OMIM gene]
- Thrombospondin II [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Intervertebral disc disease [MeSH concept]
- Intervertebral disc disorder [MedDRA Preferred Term]
- Intervertebral disc disorder (disorder) [SNOMED CT concept]
- Intervertebral disc disorder NOS [MedDRA LLT]
- Intervertebral disc disorders [ICD-9 code]
- Spinal discopathy [MedDRA LLT]
- intervertebral disc disease [MeSH Supplementary Concept]
- intervertebral disc disorder, nos [SNOMED Notion]

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