Stickler syndrome, type 5

MONDO:0013666

Any autosomal recessive Stickler syndrome in which the cause of the disease is a mutation in the COL9A2 gene.

Also known as: COL9A2 autosomal recessive Stickler syndrome, autosomal recessive Stickler syndrome caused by mutation in COL9A2, STICKLER syndrome, type V, STL5

13 clinical trials for this condition and its sub-types, 0 tagged with Stickler syndrome, type 5 itself.

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↑ Stickler syndrome (4)

Including sub-types (13) Tagged with Stickler syndrome, type 5 (0)

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