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| created at |
2024-09-19 07:43:07 UTC |
| updated at |
2024-09-23 18:19:38 UTC |
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MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
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622,528 entries
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There is 0 pattern entry.
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grand Kaine fulling syndrome
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C1860518 |
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Cerebroretinal vasculopathy, hereditary
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C1860518 |
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cerebroretinal vasculopathy, hereditary
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C1860518 |
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RVCL - retinal vasculopathy cerebral leukoencephalopathy
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C1860518 |
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autosomal dominant retinal vasculopathy with cerebral leukodystrophy
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C1860518 |
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RVCL-S - retinal vasculopathy, cerebral leukoencephalopathy, systemic manifestations
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C1860518 |
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hereditary vascular retinopathy
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C1860518 |
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Retinopathy, vascular, with cerebral and renal involvement and Raynaud and migraine phenomena
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C1860518 |
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retinopathy, vascular, with cerebral and renal involvement and Raynaud and migraine phenomena
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C1860518 |
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Vasculopathy, retinal, with cerebral leukodystrophy
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C1860518 |
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retinal vasculopathy with cerebral leukodystrophy
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C1860518 |
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vasculopathy, retinal, with cerebral leukodystrophy
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C1860518 |
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Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
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C1860518 |
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retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
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C1860518 |
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vasculopathy, retinal, with cerebral leukoencephalopathy and systemic manifestations
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C1860518 |
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