robinow syndrome

Preferred Label : robinow syndrome;

Détails

Origin ID

D4-00304;

UMLS CUI

C0265205;

Currated CISMeF NLP mapping
- Autosomal dominant Robinow syndrome [ORDO Disease]
- Robinow Syndrome [MeSH Supplementary Concept]
- Robinow Syndrome [MeSH concept]
- Robinow Syndrome [NCIt concept]
- Robinow syndrome [PASCAL descriptor]
- Robinow syndrome [DO Concept]
- Robinow syndrome [Disease (Nov.)]
- Robinow syndrome [ICD-11 More detail]
- Robinow syndrome [MedDRA Preferred Term]
- Robinow syndrome [OMIM phenotypic series]
- Robinow syndrome [ORDO Disease]
- Robinow syndrome (disorder) [SNOMED CT concept]
- Robinow syndrome, autosomal dominant 1 [OMIM Phenotype]
ICD-10 exact mapping(s)
- Congenital malformation syndromes predominantly associated with short stature [ICD-10 Sub-category (who)]
Manual BTNT mappings - CISMeF
- Autosomal dominant Robinow syndrome [ORDO Disease]
- Autosomal recessive Robinow syndrome [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Robinow syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant Robinow syndrome [ORDO Disease]
- Robinow Syndrome [MeSH concept]
- Robinow Syndrome [MeSH Supplementary Concept]
- Robinow Syndrome [NCIt concept]
- Robinow syndrome [ORDO Disease]
- Robinow syndrome [Disease (Nov.)]
- Robinow syndrome [DO Concept]
- Robinow syndrome [PASCAL descriptor]
- Robinow syndrome [MedDRA Preferred Term]
- Robinow syndrome (disorder) [SNOMED CT concept]
- Robinow syndrome, autosomal dominant 1 [OMIM Phenotype]

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