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Gordon syndrome MeSH Supplementary Concept Data 2025


MeSH Supplementary
Gordon syndrome
Unique ID
C537288
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C537288
Entry Term(s)
Arthrogryposis Multiplex Congenita, Distal, Type IIa
Arthrogryposis multiplex congenita, distal, type 2a
Arthrogryposis, distal, type 3
Camptodactyly, cleft palate, and clubfoot
Distal arthrogryposis, type 3
Registry Numbers
0
Heading Mapped to
*Arthrogryposis
*Cleft Palate
*Clubfoot
*Hand Deformities, Congenital
Frequency
20
Date of Entry
2010/08/25
Revision Date
2012/08/24
Gordon syndrome Preferred
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