Alport syndrome, recessive type MeSH Supplementary Concept Data 2024

Details
Concepts

MeSH Supplementary: Alport syndrome, recessive type
Unique ID: C536587
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536587
Registry Number: 0
Heading Mapped to: *Nephritis, Hereditary
Frequency: 1
Date of Entry: 2010/08/25

Alport syndrome, recessive type Preferred

page delivered in 0.004s