Osteodysplasia, familial, anderson type

Preferred Label : Osteodysplasia, familial, anderson type;

Type : Phenotype or locus, molecular basis unknown;

Prefixed ID : %259250;

Origin ID

259250;

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 [MeSH concept]
- osteodysplasia, familial, anderson type [MeSH Supplementary Concept]
ORDO concept(s)
- Familial osteodysplasia, Anderson type [ORDO Disease]
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 [MeSH Supplementary Concept]
- osteodysplasia, familial, anderson type [MeSH concept]