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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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agammaglobulinemia 6, autosomal recessive
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12987 |
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autosomal agammaglobulinemia caused by mutation in CD79B
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12987 |
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hereditary spherocytosis caused by mutation in EPB42
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12985 |
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hypogonadotropic hypogonadism caused by mutation in FGF8
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12988 |
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cone-rod dystrophy caused by mutation in PROM1
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12983 |
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hereditary spherocytosis caused by mutation in SLC4A1
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12981 |
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malignant germ cell neoplasm of mediastinum
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6298 |
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malignant germ cell neoplasm of the mediastinum
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6298 |
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high red cell phosphatidylcholine hemolytic anemia
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C535298 |
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leaky red cell syndrome
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C535298 |
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malignant germ cell tumor of mediastinum
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6298 |
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Dioctophyme renale caused disease or disorder
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298 |
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malignant germ cell tumor of the mediastinum
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6298 |
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mediastinal germ cell tumor, malignant
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6298 |
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HPRT complete deficiency
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10298 |
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