MeSH Browser

MeSH Supplementary: Dilution, Pigmentary
Unique ID: C566872
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566872
Entry Term(s): Albinoidism, Oculocutaneous, Autosomal Dominant
Registry Number: 0
Heading Mapped to: *Albinism, Oculocutaneous
Frequency: 23
Note: A form of oculocutaneous albinism characterized by hypopigmented hair and skin and punctate or diffuse depigmentation of the IRIS and FUNDUS OCULI without NYSTAGMUS; PHOTOPHOBIA; or visual defects. OMIM: 126070
Date of Entry: 2012/11/05
Revision Date: 2016/09/29

Dilution, Pigmentary MeSH Supplementary Concept Data 2024