Cutis laxa - Marfanoid syndrome

Preferred Label : Cutis laxa - Marfanoid syndrome;

Origin ID

467492754;

UMLS CUI

C0432335;

CISMeF manual mappings
- cutis Laxa-Marfanoid syndrome [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Cutis laxa, neonatal, with marfanoid phenotype [OMIM Phenotype]
- Cutis laxa-Marfanoid syndrome [ORDO Disease]
- Neonatal cutis laxa with marfanoid phenotype (disorder) [SNOMED CT concept]
- cutis Laxa-Marfanoid syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cutis laxa, neonatal, with marfanoid phenotype [OMIM Phenotype]
- Cutis laxa-Marfanoid syndrome [ORDO Disease]
- Neonatal cutis laxa with marfanoid phenotype (disorder) [SNOMED CT concept]
- cutis Laxa-Marfanoid syndrome [MeSH concept]
- cutis Laxa-Marfanoid syndrome [MeSH Supplementary Concept]