holt-oram syndrome

Preferred Label : holt-oram syndrome;

Details

Origin ID

D4-00906;

UMLS CUI

C0265264;

Currated CISMeF NLP mapping
- Heart-hand syndrome [ORDO Disease]
- Heart-hand syndrome type 1 [ICD-11 More detail]
- Holt Oram syndrome [Disease (Nov.)]
- Holt-Oram Syndrome [NCIt concept]
- Holt-Oram syndrome [PASCAL descriptor]
- Holt-Oram syndrome [DO Concept]
- Holt-Oram syndrome [MeSH Supplementary Concept]
- Holt-Oram syndrome [MeSH concept]
- Holt-Oram syndrome [MedDRA Preferred Term]
- Holt-Oram syndrome [ORDO Disease]
- Holt-Oram syndrome (disorder) [Inactive SNOMED CT concept]
- Holt-Oram syndrome (disorder) [SNOMED CT concept]
- Holt-oram syndrome [OMIM Phenotype]
ICD-10 exact mapping(s)
- Congenital malformation syndromes predominantly involving limbs [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Non-syndromic limb reduction defect [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Holt-Oram syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Heart-hand syndrome [ORDO Disease]
- Heart-hand syndrome type 1 [ICD-11 More detail]
- Holt Oram syndrome [Disease (Nov.)]
- Holt-Oram Syndrome [NCIt concept]
- Holt-Oram syndrome [MeSH concept]
- Holt-Oram syndrome [MeSH Supplementary Concept]
- Holt-Oram syndrome [ORDO Disease]
- Holt-Oram syndrome [MedDRA Preferred Term]
- Holt-Oram syndrome [DO Concept]
- Holt-Oram syndrome [PASCAL descriptor]
- Holt-Oram syndrome (disorder) [SNOMED CT concept]
- Holt-oram syndrome [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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