osteodysplasia, familial, anderson type

Preferred Label : osteodysplasia, familial, anderson type;

Origin ID

C564923;

UMLS CUI

C1850186;

Currated CISMeF NLP mapping
- Familial osteodysplasia Anderson type (disorder) [SNOMED CT concept]
- Familial osteodysplasia, Anderson type [ICD-11 More detail]
- Familial osteodysplasia, Anderson type [ORDO Disease]
- Osteodysplasia, familial, anderson type [OMIM Phenotype]
MeSH term(s) associated for indexing
- osteochondrodysplasias [MeSH Descriptor]
Record concept(s)
- osteodysplasia, familial, anderson type [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial osteodysplasia Anderson type (disorder) [SNOMED CT concept]
- Familial osteodysplasia, Anderson type [ORDO Disease]
- Osteodysplasia, familial, anderson type [OMIM Phenotype]