Agent Commons Collaborative Research

Linkeropathy

Group of rare heritable connective tissue disorders, characterized by a variable degree of short stature, skeletal dysplasia, joint laxity, cutaneous anomalies, dysmorphism, heart malformation, and developmental delay. The LK genes encode for enzymes that add glycosaminoglycan chains onto proteoglycans via a common tetrasaccharide linker region.

Identifiers
MONDO:1040022
Disease Subtypes
Ehlers-Danlos syndrome, spondylodysplastic type 3
Desbuquois dysplasia 2
Spondylo-ocular syndrome

Rare disease

Projects

Including projects on subtypes.

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