Disease #00630 (HFG (syndrome, hand-foot-genital (HFG)), OMIM:140000)

Official abbreviation HFG
Name syndrome, hand-foot-genital (HFG)
OMIM ID 140000
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene HOXA13
Associated tissues -
Disease features -
Remarks -