alport syndrome

Preferred Label : alport syndrome;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0483241;

UMLS CUI

C1567741;

Currated CISMeF NLP mapping
- Alport Syndrome [NCIt concept]
- Alport syndrome [PASCAL descriptor]
- Alport syndrome [DO Concept]
- Alport syndrome [Disease (Nov.)]
- Alport syndrome [ICD-11 More detail]
- Alport syndrome [OMIM phenotypic series]
- Alport syndrome [ORDO Disease]
- Alport syndrome (disorder) [SNOMED CT concept]
- Alport's syndrome [MedDRA Preferred Term]
- Alport's syndrome (disorder) [Inactive SNOMED CT concept]
- Hereditary nephritis (disorder) [SNOMED CT concept]
- Other specified congenital malformation syndromes, not elsewhere classified [ICD-10 Sub-category]
- Other specified congenital malformation syndromes, not elsewhere classified [ICD-10 Sub-category (who)]
- hereditary nephritis [SNOMED Notion]
Related record
- nephritis, hereditary [MeSH Descriptor]
See also inter- (CISMeF)
- Zellweger syndrome [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Alport Syndrome [NCIt concept]
- Alport syndrome [ORDO Disease]
- Alport syndrome (disorder) [SNOMED CT concept]
- Alport's syndrome [MedDRA Preferred Term]
Validated automatic mappings to NTBT
- hereditary nephritis [Disease (Nov.)]