Gene: [05q1/ERVR] Wagner syndrome; erosive vitreoretinopathy; [WGN1 ]

CAG

Brown-1995 demonstrated that erosive vitreoretinopathy and Wagner disease are allelic disorders and genetically distinct from COL2A1-associated Stickler syndrome (GEM:12q131/COL2A1). Authors mapped the disease phenotype to Chr 5q13-14."

REF

LIN,LOC "Brown DM &: Arch Ophthal, 113, N5, 671-675, 1995

CLA

unknown, basic

LOC

05 q13-14

MIM

MIM: 143200

SYN

WGN1