Cartilage Development Disorder

Preferred Label : Cartilage Development Disorder;

NCIt synonyms : Chondrodystrophy;

NCIt definition : Any dysfunction in the growth of cartilage.;

Details

Origin ID

C34466;

UMLS CUI

C0008449;

Automatic exact mappings (from CISMeF team)
- Chondrodystrophy [MedDRA LLT]
- osteochondrodysplasia [DO Concept]
Currated CISMeF NLP mapping
- CHONDRODYSTROPHY [WHO-ART Preferred Term]
- Cartilage development disorder [MedDRA Preferred Term]
- Cartilage development disorder NOS [MedDRA LLT]
- Chondrodystrophy [MedDRA Preferred Term]
- Chondrodystrophy [ICD-9 code]
- Congenital anomaly of cartilage (disorder) [SNOMED CT concept]
- Disorder cartilage development (NOS) [MedDRA LLT]
- chondrodystrophy [Disease (Nov.)]
DO Cross reference
- osteochondrodysplasia [DO Concept]
Has associated anatomic sites
- Bone [NCIt concept]
- Connective and Soft Tissue [NCIt concept]
- Musculoskeletal System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- CHONDRODYSTROPHY [WHO-ART Preferred Term]
- Cartilage development disorder [MedDRA Preferred Term]
- Cartilage development disorder NOS [MedDRA LLT]
- Chondrodystrophy [ICD-9 code]
- Chondrodystrophy [MedDRA Preferred Term]
- Chondrodystrophy [MedDRA LLT]
- Congenital anomaly of cartilage (disorder) [SNOMED CT concept]
- Disorder cartilage development (NOS) [MedDRA LLT]
- chondrodystrophy [Disease (Nov.)]
- congenital anomaly of cartilage, nos [SNOMED Notion]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_has_normal_tissue_origin
- Connective and Soft Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Bone [NCIt concept]

Keyword's position in hierarchy(ies) :

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