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| created at |
2017-12-28 15:45:48 UTC |
| updated at |
2017-12-28 18:31:12 UTC |
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Sub-category as a label
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520,470 entries
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There is 0 pattern entry.
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DFNB63
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DISO:Disease or Syndrome |
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DEAFNESS, AUTOSOMAL RECESSIVE 63
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DISO:Disease or Syndrome |
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DFNB63
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DISO:Disease or Syndrome |
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Deafness, Autosomal Recessive 63
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DISO:Disease or Syndrome |
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DEAFNESS, AUTOSOMAL RECESSIVE 63
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DISO:Disease or Syndrome |
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Tachycardia (hereditary coproporphyria, HCP)
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DISO:Finding |
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Caused by mutation in the nephrocystin 3 gene (NPHP3, 608002.0001)
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DISO:Finding |
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OSTEOGENESIS IMPERFECTA, TYPE V
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DISO:Disease or Syndrome |
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OI, Type V
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DISO:Disease or Syndrome |
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Osteogenesis Imperfecta, Type V
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DISO:Disease or Syndrome |
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OI5
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DISO:Disease or Syndrome |
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OI5
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DISO:Disease or Syndrome |
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OSTEOGENESIS IMPERFECTA, TYPE V
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DISO:Disease or Syndrome |
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OI, TYPE V
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DISO:Disease or Syndrome |
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Normal ribs
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DISO:Finding |
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