MeSH Browser

MeSH Supplementary: Ermine phenotype
Unique ID: C535508
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535508
Entry Term(s): Cutaneous albinism hermine phenotype; O'Doherty syndrome; Pigmentary disorder with hearing loss
Registry Number: 0
Heading Mapped to: *Hearing Loss, Sensorineural; *Piebaldism
Frequency: 2
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Concept UI: M0529969
Registry Number: 0
Terms: Ermine phenotype Preferred Term
Term UI T736332
Date02/24/2009
LexicalTag NON
ThesaurusID; Pigmentary disorder with hearing loss
Term UI T736335
Date02/24/2009
LexicalTag NON
ThesaurusID; O'Doherty syndrome
Term UI T752050
Date06/01/2009
LexicalTag NON
ThesaurusID ORD (2010); Cutaneous albinism hermine phenotype
Term UI T736333
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010)

Ermine phenotype MeSH Supplementary Concept Data 2024