fibrous dysplasia, polyostotic

Preferred Label : fibrous dysplasia, polyostotic;

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

Origin ID

M0008457;

UMLS CUI

C0016065;

Automatic exact mappings (from CISMeF team)
- Polyostotic fibrous dysplasia [ICD-11 More detail]
- polyostotic fibrous dysplasia [Radlex concept]
Currated CISMeF NLP mapping
- McCune Albright syndrome [DO Concept]
- Mccune-albright syndrome [OMIM Phenotype]
- Polyostotic Fibrous Dysplasia [NCIt concept]
- Polyostotic fibrous dysplasia [ICD-10 Sub-category]
- Polyostotic fibrous dysplasia [ICD-10 Sub-category (who)]
- Polyostotic fibrous dysplasia [HPO term]
- Polyostotic fibrous dysplasia [ORDO Disease]
- Polyostotic fibrous dysplasia of bone (disorder) [SNOMED CT concept]
- polyostotic fibrous dysplasia of bone, nos [SNOMED Notion]
MeSH narrower concept(s)
- albright syndrome [MeSH concept]
Related record
- fibrous dysplasia, polyostotic [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Albright disease [PASCAL descriptor]
- McCune Albright syndrome [DO Concept]
- Polyostotic Fibrous Dysplasia [NCIt concept]
- Polyostotic fibrous dysplasia [ORDO Disease]
- Polyostotic fibrous dysplasia [ICD-10 Sub-category]
- Polyostotic fibrous dysplasia [HPO term]
- Polyostotic fibrous dysplasia [ICD-10 Sub-category (who)]
- Polyostotic fibrous dysplasia of bone [MedDRA LLT]
- Polyostotic fibrous dysplasia of bone [ICD-9 code]
- Polyostotic fibrous dysplasia of bone (disorder) [SNOMED CT concept]
- polyostotic fibrous dysplasia of bone, nos [SNOMED Notion]