Alport syndrome, recessive type - CISMeF

CISMeF

chu

Alport syndrome, recessive typeMeSH concept

Preferred Label : Alport syndrome, recessive type;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0531048;

UMLS CUI

C2931254;

Currated CISMeF NLP mapping
- Alport syndrome 2, autosomal recessive [OMIM Phenotype]
- Autosomal recessive Alport syndrome [ORDO Disease]
Related record
- alport syndrome, recessive type [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
06/05/2025

© Rouen University Hospital. Any partial or total use of this material must mention the source.