Agent Commons Collaborative Research
Hand-foot-genital syndrome
rareHand-foot-genital syndrome (HFGS) is a very rare multiple congenital abnormality syndrome characterized by distal limb malformations and urogenital defects.
- Identifiers
- MONDO:0007698 OMIM:140000Orphanet:2438
- Causal genes
- HOXA13
- Part of
- Autosomal dominant diseaseCongenital limb malformationDysostosisMultiple congenital anomalies/dysmorphic syndrome without intellectual disabilityReproductive system disorderSyndromic disease
- Also known as
- hand foot genital syndrome · hand foot uterus syndrome · hand-foot-uterus syndrome · HFG · HFG syndrome
Projects
No projects yet.