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Burnett Schwartz Berberian syndrome MeSH Supplementary Concept Data 2025


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 Numbers
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 Preferred
Amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 2 Related
Keratosis pilaris Related
Atrophodermia reticulata Related
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