The following pages link to Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Autosomal dominant retinal vasculopathy with cerebral leukodystrophy (redirect page) (links | edit)
- Cerebroretinal vasculopathy (redirect page) (links | edit)
- List of diseases (C) (links | edit)
- User:AlexNewArtBot/GeneticsSearchResult/archive1 (links | edit)
- User:AlexNewArtBot/NeuroscienceSearchResult/archive2 (links | edit)
- User:AlexNewArtBot/MedicineSearchResult/archive22 (links | edit)
- User:AlexNewArtBot/ReferencesSearchResult/archive33 (links | edit)
- User:Davidruben/OrphaNet (links | edit)
- User talk:Anandks007/Med (links | edit)
- Hereditary cerebroretinal vasculopathy (redirect page) (links | edit)
- Grand-Kaine-Fulling syndrome (redirect page) (links | edit)
- Grand Kaine Fulling syndrome (redirect page) (links | edit)
- Talk:Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations (transclusion) (links | edit)
- User talk:DNA.scientist (links | edit)
- Misplaced Pages:WikiProject Medicine/Lists of pages/Articles (links | edit)
- Misplaced Pages:WikiProject Medicine/The ICD-11 coding challenge/6200–6299 (links | edit)