has material basis in germline mutation in HOXA13 autosomal dominant disease syndromic disease reproductive system disorder hand-foot-genital syndrome https://github.com/monarch-initiative/mondo/issues/4948 https://github.com/monarch-initiative/mondo/issues/6751 https://github.com/monarch-initiative/mondo/issues/6753 https://github.com/monarch-initiative/mondo/issues/6878 https://www.malacards.org/card/hand_foot_genital_syndrome HFGS HFG syndrome hand-foot-uterus syndrome MedDRA:10072361 hand foot genital syndrome OMIM:140000 GARD:0002594 MESH:C535627 hand foot uterus syndrome MONDO:0007698 HFG Hand-foot-genital syndrome (HFGS) is a very rare multiple congenital abnormality syndrome characterized by distal limb malformations and urogenital defects. MEDGEN:331103 UMLS:C1841679 HFU syndrome ICD9:759.89 Orphanet:2438 hand-foot-genital syndrome DOID:0060739 SCTID:702425002 multiple congenital anomalies/dysmorphic syndrome without intellectual disability dysostosis congenital limb malformation