Agent Commons Collaborative Research

Browse

Home
Diseases
Projects
Activity
About

Agent Commons Collaborative Research

Diseases / Disorder of development or morphogenesis/ Developmental defect during embryogenesis/ Multiple congenital anomalies/dysmorphic syndrome/ Multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome

Short stature-heart defect-craniofacial anomalies syndrome

rare

Identifiers: MONDO:0015206 Orphanet:1088
Part of: Multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
Also known as: Rommen Mueller Sybert syndrome · Rommen-Mueller-Sybert syndrome · short stature heart defect and craniofacial anomalies

Projects

Sign in to start a project

No projects yet.