dyschondroplasias

Preferred Label : dyschondroplasias;

UMLS semantic type : T019 - Congenital Abnormality; T047 - Disease or Syndrome;

Origin ID

M0015521;

UMLS CUI

C0013366;

Automatic exact mappings (from CISMeF team)
- Des-Gamma Carboxyprothrombin [NCIt concept]
- Enchondromatosis [NCIt concept]
- Enchondromatosis, multiple, ollier type [OMIM Phenotype]
- Ollier disease [ORDO Disease]
- Ollier disease [DO Concept]
- Paraneoplastic neurologic syndrome [ORDO Disease]
- Primary ciliary dyskinesia [ORDO Disease]
- osteochondromatosis syndrome [SNOMED Notion]
Currated CISMeF NLP mapping
- Dyschondroplasia [NCIt concept]
- Dyschondroplasia [MedDRA LLT]
Related record
- osteochondrodysplasias [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Dyschondroplasia [MedDRA LLT]
- Dyschondroplasia [NCIt concept]