Craniomicromelic syndrome

Preferred Label : Craniomicromelic syndrome;

Type : Other, mainly phenotypes with suspected mendelian basis;

Prefixed ID : 602558;

Origin ID

602558;

UMLS CUI

C1865184;

Currated CISMeF NLP mapping
- Craniomicromelic syndrome [ICD-11 More detail]
- Craniomicromelic syndrome [ORDO Disease]
- Craniomicromelic syndrome (disorder) [SNOMED CT concept]
- craniomicromelic syndrome [MeSH concept]
- craniomicromelic syndrome [MeSH Supplementary Concept]
ORDO concept(s)
- Craniomicromelic syndrome [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Craniomicromelic syndrome [ORDO Disease]
- Craniomicromelic syndrome (disorder) [SNOMED CT concept]
- craniomicromelic syndrome [MeSH Supplementary Concept]
- craniomicromelic syndrome [MeSH concept]