- OMIM ID
-
192315
- OMIM term:
- VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL
- Alternative terms:
-
CEREBRORETINAL VASCULOPATHY, HEREDITARY; CRV
RETINOPATHY, VASCULAR, WITH CEREBRAL AND RENAL INVOLVEMENT AND RAYNAUD AND MIGRAINE PHENOMENA
- (∗) Location:
- 3p21.31
- (†) Associated OMIM genes:
- TREX1
- (‡) Associated MGI genes:
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