radioulnar synostosis, nonsyndromic, susceptibility to
http://purl.obolibrary.org/obo/MONDO_0100183
A susceptibility or predisposition to radioulnar synostosis in which the cause of the disease is a mutation in the SMAD6 gene. [ MONDO:patterns/susceptibility_by_gene ]
Term info
database cross reference
- OMIM:179300 (MONDO:equivalentTo)
created by
http://orcid.org/0000-0001-5208-3432
definition
A susceptibility or predisposition to radioulnar synostosis in which the cause of the disease is a mutation in the SMAD6 gene.
exactMatch
https://omim.org/entry/179300
id
MONDO:0100183