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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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congenital alopecia and nail dystrophy T-cell immunodeficiency
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C536781 |
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congenital alopecia, and nail dystrophy t-cell immunodeficiency
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C536781 |
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zonular cataract and nystagmus
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C536727 |
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muscle atrophy, and oculomotor apraxia contractures of feet
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C536703 |
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cleft lip and palate, mental retardation, and syndactyly ectodermal dysplasia
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C536726 |
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anal anomalies, and porokeratosis craniosynostosis
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C536789 |
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wilms tumor and radial bilateral aplasia
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C536707 |
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hereditary iron-loading anemia
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C536761 |
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hereditary sideroblastic anemia
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C536761 |
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sideroblastic, x-linked anemia
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C536761 |
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systemic necrotizing angiitis
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C536779 |
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systemic necrotizing angitis
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C536779 |
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hearing loss ankle anomalies and neurological regression-dementia
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C536749 |
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craniosynostosis radial aplasia syndrome
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C536788 |
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bilateral radial aplasia with wilms tumor
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C536707 |
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