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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.
seizures, benign familial infantile, type 3
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11904 |
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juvenile myelomonocytic leukemia
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11908 |
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juvenile chronic myeloid leukemia
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11908 |
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leukemia, chronic myelomonocytic
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11908 |
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leukemia, juvenile myelomonocytic
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11908 |
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juvenile chronic myelomonocytic leukemia
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11908 |
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Charcot-Marie-Tooth disease type 1F
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11902 |
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deficient DNA repair
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21190 |
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disorder, DNA repair-deficiency
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21190 |
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disorders, DNA repair-deficiency
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21190 |
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porokeratosis, disseminated superficial actinic, 2
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11900 |
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3-alpha beta-hydroxy-delta-5-C27-steroid oxidoreductase, deficiency of
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11906 |
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chromosome instability syndrome
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21190 |
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chromosome instability syndromes
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21190 |
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bile acid synthesis defect, congenital, 1
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11906 |
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