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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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AKAP9 long QT syndrome
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12738 |
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Sex reversion-kidneys, adrenal and lung dysgenesis syndrome
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12734 |
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familial thoracic aortic aneurysm and aortic dissection caused by mutation in ACTA2
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12730 |
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familial thoracic aortic aneurysm with livedo reticularis and iris flocculi
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12730 |
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autosomal recessive bestrophinopathy
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12733 |
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leiomyoma of ciliary body
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21273 |
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microtia eye coloboma and imperforation of the nasolacrimal duct
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12739 |
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dilatation of colon
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1273 |
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severe intellectual disability and absent nails of hallux and pollex
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12735 |
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severe intellectual disability-aplasia/hypoplasia of thumb and hallux syndrome
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12735 |
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SLC29A3 spectrum disorder
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11273 |
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disorder, sex differentiation
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D012734 |
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disorder, sexual differentiation
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D012734 |
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disorders, sex differentiation
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D012734 |
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disorders, sexual differentiation
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D012734 |
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