Ochronosis, hereditary MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Ochronosis, hereditary
Unique ID: C537862
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537862
Entry Term(s): Hereditary ochronosis
Registry Numbers: 0
Heading Mapped to: *Ochronosis
Frequency: 13
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

Ochronosis, hereditary Preferred

page delivered in 0.004s