Phenotypes for disease #00887 (RVCL (vasculopathy, retinal, with cerebral leukodystrophy (RVCL)), OMIM:192315)

7 entries on 1 page. Showing entries 1 - 7.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000087931 retinal vasculopathy with cerebral leukodystrophy - - Unknown - - - - - Boukje de Vries 00112367
0000087932 retinal vasculopathy with cerebral leukodystrophy - - Unknown - - - - - Boukje de Vries 00112368
0000087934 retinal vasculopathy with cerebral leukodystrophy - - Unknown - - - - - Boukje de Vries 00112370
0000087936 retinal vasculopathy with cerebral leukodystrophy - - Unknown - - - - - Boukje de Vries 00112372
0000087937 retinal vasculopathy with cerebral leukodystrophy - - Unknown - - - - - Boukje de Vries 00112373
0000087943 Retinal Vasculopathy with Cerebral Leukodystrophy - - Unknown - - - - - Boukje de Vries 00112379
0000242050 Cerebral microangiopathy; unclear WML and suspected migraine headache DD CADASIL - - Unknown 50y - - - - Andreas Laner 00320006
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