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MIM:614500 - CONE-ROD DYSTROPHY 16; CORD16
Xenbase Genes: cfap418
Human Disease Resource: MIM
MONDO:0013786 - cone-rod dystrophy 16 |
MONDO:0015993 - cone-rod dystrophy |
MONDO:0019200 - retinitis pigmentosa |
DOID:0111022 - cone-rod dystrophy 16 |
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MONDO:0013786 - cone-rod dystrophy 16 |
MONDO:0015993 - cone-rod dystrophy |
MONDO:0019200 - retinitis pigmentosa |
DOID:0111022 - cone-rod dystrophy 16 |