MeSH Browser

MeSH Supplementary: Burnett Schwartz Berberian syndrome
Unique ID: C537412
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537412
Entry Term(s): Amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 2; Atrophodermia Reticulata Symmetrica Faciei; Atrophodermia reticulata; Atrophodermia vermiculata; Folliculitis ulerythematosa; Folliculitis ulerythematosa reticulata; Honeycomb atrophy; Keratosis Pilaris Atrophicans Facies; Keratosis pilaris; Ulerythema ophryogenes; Ulerythema ophryogenes with multiple congenital anomalies; Ulerythema ophryogenesis
Registry Number: 0
Heading Mapped to: *Abnormalities, Multiple; Eyebrows / *abnormalities; *Darier Disease
Frequency: 140
Note: Keratosis pilaris affecting the follicles of the eyebrow hairs
Date of Entry: 2010/08/25
Revision Date: 2015/11/09

Burnett Schwartz Berberian syndrome MeSH Supplementary Concept Data 2024