hecht scott syndrome

Preferred Label : hecht scott syndrome;

MeSH note : Terminal transverse defects of the limbs associated with congenital heart malformations;

MeSH synonym : limb deficiency-heart malformation syndrome;

Details

Origin ID

C535856;

UMLS CUI

C2931047;

Currated CISMeF NLP mapping
- FATCO syndrome [ORDO Disease]
- Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome [OMIM Phenotype]
- Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- abnormalities, multiple [MeSH Descriptor]
- craniofacial abnormalities [MeSH Descriptor]
- hand deformities, congenital [MeSH Descriptor]
- heart defects, congenital [MeSH Descriptor]
Record concept(s)
- Hecht Scott syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- FATCO syndrome [ORDO Disease]

Keyword's position in hierarchy(ies) :

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