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| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
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MONDO_bioport_pref_name
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183,974 entries
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There is 0 pattern entry.
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neuropathy, hereditary sensory radicular, autosomal dominant
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D009477 |
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neuropathy, hereditary sensory, type i
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D009477 |
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apple peel syndrome with microcephaly and ocular anomalies
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9477 |
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familial dysautonomia, type II
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D009477 |
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acroosteolysis, giaccai type
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D009477 |
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jejunal atresia with microcephaly and ocular anomalies
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9477 |
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HSAN type v
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D009477 |
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congenital sensory, with anhidrosis neuropathy
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D009477 |
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pain insensitivity with anhidrosis, congenital
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D009477 |
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hereditary sensory, type i neuropathy
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D009477 |
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