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MIM:613829 - LEBER CONGENITAL AMAUROSIS 7; LCA7
Xenbase Genes: crx
Human Disease Resource: MIM
MONDO:0013449 - Leber congenital amaurosis 7 |
MONDO:0018998 - Leber congenital amaurosis |
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MONDO:0013449 - Leber congenital amaurosis 7 |
MONDO:0018998 - Leber congenital amaurosis |