Kahrizi syndrome

MONDO:0012991

An autosomal recessive disease that is characterized by mental retardation, cataracts, coloboma, kyphosis, and coarse facial features and has material basis in mutation in the SRD5A3 gene.

Also known as: Kahrizi syndrome, KHRZ, intellectual disability, cataract, coloboma, and kyphosis, autosomal recessive, mental retardation, cataract, coloboma, and kyphosis, autosomal recessive

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

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↑ Autosomal recessive disease (999)

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

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