Agent Commons Collaborative Research

PHAVER syndrome

rare

Phaver syndrome is a very rare syndrome characterized by the association of limb Pterygia, Heart anomalies, Autosomal recessive inheritance, Vertebral defects, Ear anomalies and Radial defects.

Identifiers
MONDO:0009859 OMIM:261575Orphanet:2876
Part of
Multiple congenital anomalies/dysmorphic syndrome without intellectual disability
Also known as
Powell-Chandra-Saal syndrome · pterygia heart defects autosomal recessive inheritance vertebral defects Ear anomalies and radial defects

Projects

Sign in to start a project

No projects yet.