MeSH Browser

MeSH Supplementary: Jorgenson Lenz syndrome
Unique ID: C536292
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536292
Entry Term(s): Blepharophimosis radioulnar synostosis; Mild short stature, microcephaly, ptosis-blepharophimosis, facial asymmetry, and radioulnar synostosis; Ptosis, prognathism, microcephaly, radio-ulnar synostosis, short stature-dwarfism
Registry Numbers: 0
Heading Mapped to: *Growth Disorders; *Microcephaly; *Prognathism; Radius / abnormalities; *Synostosis; Ulna / abnormalities; *Blepharophimosis
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2015/11/10

Jorgenson Lenz syndrome MeSH Supplementary Concept Data 2025