guttmacher syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Guttmacher syndrome is an extremely rare syndrome characterized by hypoplastic thumbs and halluces, 5th finger clinobrachydactyly, postaxial polydactyly of the hands, short or uniphalangeal 2nd toes with absent nails and hypospadias. (Orphanet Rare Disease Ontology, Orphanet_2957)
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1 genes associated with the guttmacher syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
HOXA13 homeobox A13