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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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Smith McCort dysplasia
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15799 |
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familial spondyloepiphyseal dysplasia
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C535799 |
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chromosome 3-linked frontotemporal dementia
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C579991 |
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microcephaly primary hereditary
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C579935 |
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atelosteogenesis type iii
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C579928 |
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catsper-related nonsyndromic male infertility
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C579978 |
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catsper1-related nonsyndromic male infertility
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C579978 |
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sensory ataxia neuropathy dysarthria and ophthalmoplegia
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C579922 |
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recessive ataxia of beauce
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C579934 |
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ornithinemia with gyrate atrophy
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D015799 |
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chmp2b-related amyotrophic lateral sclerosis
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C579991 |
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gyrate atrophy of the choroid and retina
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D015799 |
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amyotrophic lateral sclerosis, chmp2b-related
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C579991 |
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childhood myocerebrohepatopathy spectrum
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C579990 |
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spondyloperipheral dysplasia short ulna
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C535799 |
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