thomas syndrome

Preferred Label : thomas syndrome;

Origin ID

C536514;

UMLS CUI

C2931225;

Automatic exact mappings (from CISMeF team)
- Olivopontocerebellar degeneration (disorder) [SNOMED CT concept]
- olivopontocerebellar atrophy [DO Concept]
Currated CISMeF NLP mapping
- Potter sequence cleft lip and palate cardiopathy syndrome (disorder) [SNOMED CT concept]
- Thomas syndrome [ORDO Disease]
MeSH term(s) associated for indexing
- abnormalities, multiple [MeSH Descriptor]
- cleft lip [MeSH Descriptor]
- heart defects, congenital [MeSH Descriptor]
- kidney [MeSH Descriptor]
- palate [MeSH Descriptor]
ORDO relation(s)
- Thomas syndrome [ORDO Disease]
Record concept(s)
- Thomas syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Potter sequence cleft lip and palate cardiopathy syndrome (disorder) [SNOMED CT concept]
- Thomas syndrome [ORDO Disease]