Phenotypes
Db Link Name Definition Comment Is a
HPO HP:0000007 Autosomal recessive inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in individuals with two pathogenic alleles, either homozygotes (two copies of the same mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:probinson] — HP:0000005
HPO HP:0009374 Broad phalanges of the 5th finger "Increased width of the phalanges of the 5th finger." [HPO:curators] — HP:0004213, HP:0009768
HPO HP:0001162 Postaxial hand polydactyly "Supernumerary digits located at the ulnar side of the hand (that is, on the side with the fifth finger)." [HPO:sdoelken] — HP:0001161, HP:0004207, HP:0100259
OMIM OMIM:615226 POLYDACTYLY, POSTAXIAL, TYPE A6; PAPA6 — — —