|
DOID:0090021 - split hand-foot malformation 1
Disease Ontology Definition:A split-hand/foot malformation that has_material_basis_in contiguous gene mutations caused by deletion, duplication, or rearrangement of chromosome 7q21.3 involving the DSS1, DLX5, and DLX6 genes and possible regulatory elements in the region.
Synonyms: SHFD1, SHFM1,
Echinobase Genes :
MIM:183600 - split-hand/foot malformation 1; shfm1 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
split hand-foot malformation (is_a)