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Jorgenson Lenz syndrome MeSH Supplementary Concept Data 2025


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 Preferred
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