MeSH Browser

MeSH Supplementary: Heterochromia iridis
Unique ID: C538115
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538115
Entry Term(s): Asymmetry in the pigmentation of the irides; Pigmentary abnormality of the anterior segment of the eye
Registry Numbers: 0
Heading Mapped to: *Iris Diseases; *Pigmentation Disorders
Frequency: 63
Note: Asymmetry of iris pigmentation. It may occur in cases of HORNER SYNDROME; WAARDENBURG SYNDROME; or PIEBALDISM. OMIM: 142500
Date of Entry: 2024/11/05
Revision Date: 2024/11/05

Heterochromia iridis MeSH Supplementary Concept Data 2025