MeSH Browser

MeSH Supplementary: Krieble Bixler syndrome
Unique ID: C537619
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537619
Entry Term(s): Autosomal dominant blepharophimosis with multiple congenital anomalies
Registry Numbers: 0
Heading Mapped to: *Abnormalities, Multiple; *Blepharophimosis
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

Krieble Bixler syndrome MeSH Supplementary Concept Data 2025