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MIM:613826 - LEBER CONGENITAL AMAUROSIS 6; LCA6
Xenbase Genes: rpgrip1
Human Disease Resource: MIM
MONDO:0013446 - Leber congenital amaurosis 6 |
MONDO:0018998 - Leber congenital amaurosis |
DOID:0110329 - Leber congenital amaurosis 6 |
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MONDO:0013446 - Leber congenital amaurosis 6 |
MONDO:0018998 - Leber congenital amaurosis |
DOID:0110329 - Leber congenital amaurosis 6 |