PHAVER syndrome

MONDO:0009859

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.

Also known as: PHAVER syndrome, Powell-Chandra-Saal syndrome, pterygia heart defects autosomal recessive inheritance vertebral defects Ear anomalies and radial defects

0 clinical trials for this condition and its sub-types, 0 tagged with PHAVER syndrome itself.

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Part of

↑ Multiple congenital anomalies/dysmorphic syndrome without intellectual disability (163)

Including sub-types (0) Tagged with PHAVER syndrome (0)

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