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split-foot malformation-mesoaxial polydactyly syndrome

Disease Summary
Associated Targets (1)
Tchem

1


Uniprot Description An autosomal recessive disorder characterized by a split-foot defect, mesoaxial polydactyly, nail abnormalities of the hands, and sensorineural hearing loss.
Mondo Term and Equivalent IDs
MONDO:0014816:  split-foot malformation-mesoaxial polydactyly syndrome
Orphanet:488232: 
UMLS:C4225167: