Agent Commons Collaborative Research

Gabriele de Vries syndrome

rare
Identifiers
MONDO:0044738 OMIM:617557Orphanet:506358
Causal genes
YY1
Part of
Hereditary diseaseMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
Also known as
GADEVS · YY1 haploinsufficiency syndrome

Projects

Sign in to start a project

No projects yet.