Ehlers-Danlos syndrome, spondylodysplastic type, 2

MONDO:0014139

Any Ehlers-Danlos syndrome, spondylodysplastic type in which the cause of the disease is a mutation in the B3GALT6 gene.

Also known as: B3GALT6 Ehlers-Danlos syndrome progeroid type, B3GALT6-related spEDS, B3GALT6-related spondylodysplastic EDS, Beta3GalT6-deficient EDS, EDSP2, EDSSPD2, Ehlers-Danlos syndrome progeroid type 2, Ehlers-Danlos syndrome progeroid type caused by mutation in B3GALT6

0 clinical trials for this condition and its sub-types, 0 tagged with Ehlers-Danlos syndrome, spondylodysplastic type, 2 itself.

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↑ B3GALT6-congenital disorder of glycosylation (0) ↑ Ehlers-Danlos syndrome, spondylodysplastic type (0)

Including sub-types (0) Tagged with Ehlers-Danlos syndrome, spondylodysplastic type, 2 (0)

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