cone-rod dystrophy 19 (Q32146216)
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cone-rod dystrophy that has material basis in homozygous or compound heterozygous mutation in the TTLL5 gene on chromosome 14q24
- CORD19
- cone-rod dystrophy type 19
- CONE-ROD DYSTROPHY 19
- CONE-ROD DYSTROPHY 19; CORD19
Language | Label | Description | Also known as |
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English | cone-rod dystrophy 19 |
cone-rod dystrophy that has material basis in homozygous or compound heterozygous mutation in the TTLL5 gene on chromosome 14q24 |
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