seckel syndrome

Preferred Label : seckel syndrome;

Origin ID

D4-00208;

UMLS CUI

C0265202;

Automatic exact mappings (from CISMeF team)
- Congenital malformation syndromes predominantly associated with short stature [ICD-10 Sub-category (who)]
- Seckel syndrome [ICD-11 More detail]
- Seckel syndrome [OMIM phenotypic series]
Currated CISMeF NLP mapping
- Seckel Syndrome [NCIt concept]
- Seckel syndrome [PASCAL descriptor]
- Seckel syndrome [DO Concept]
- Seckel syndrome [ORDO Disease]
- Seckel syndrome (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Congenital malformation syndromes predominantly associated with short stature [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Slender bone dysplasia [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Seckel syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Seckel Syndrome [NCIt concept]
- Seckel syndrome [ORDO Disease]
- Seckel syndrome [DO Concept]
- Seckel syndrome [PASCAL descriptor]
- Seckel syndrome (disorder) [SNOMED CT concept]
- Seckel syndrome 1 [OMIM Phenotype]
- Seckel syndrome 1 [MeSH concept]