septo-optic dysplasia sequence

Preferred Label : septo-optic dysplasia sequence;

Details

Origin ID

D4-01523;

UMLS CUI

C0338503;

Automatic exact mappings (from CISMeF team)
- Septo-optic dysplasia [ICD-11 More detail]
Currated CISMeF NLP mapping
- Septo-Optic Dysplasia [NCIt concept]
- Septo-Optic dysplasia [MeSH concept]
- Septo-optic dysplasia [ICD-10 Sub-category (who)]
- Septo-optic dysplasia [HRDO Sign]
- Septo-optic dysplasia [HPO term]
- Septo-optic dysplasia [MedDRA Preferred Term]
- Septo-optic dysplasia of brain [ICD-10 Sub-category]
- Septo-optic dysplasia sequence (disorder) [SNOMED CT concept]
- Septooptic dysplasia [OMIM Phenotype]
- Septooptic dysplasia [PASCAL descriptor]
- septo-optic dysplasia [Disease (Nov.)]
- septo-optic dysplasia [MeSH Descriptor]
- septooptic dysplasia [DO Concept]
ICD-10 exact mapping(s)
- Other specified congenital malformations of eye [ICD-10 Sub-category (who)]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Septo-optic dysplasia sequence (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Septo-Optic Dysplasia [NCIt concept]
- Septo-Optic dysplasia [MeSH concept]
- Septo-optic dysplasia [MedDRA Preferred Term]
- Septo-optic dysplasia [HPO term]
- Septo-optic dysplasia [HRDO Sign]
- Septo-optic dysplasia [ICD-10 Sub-category (who)]
- Septo-optic dysplasia sequence (disorder) [SNOMED CT concept]
- Septooptic dysplasia [OMIM Phenotype]
- Septooptic dysplasia [PASCAL descriptor]
- de Morsier's syndrome [MedDRA LLT]
- septo-optic dysplasia [MeSH Descriptor]
- septooptic dysplasia [DO Concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients