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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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desiccytosis, hereditary
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C536764 |
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hereditary desiccytosis
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C536764 |
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Aprosencephaly-atelencephaly syndrome
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C536767 |
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XK syndrome
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C536767 |
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garcia-lurie syndrome
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C536767 |
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anemia, sex-linked hypochromic sideroblastic
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C536761 |
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wittwer tpe X-linked mental retardation syndrome
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C536760 |
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congenital sideroblastic anaemia
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C536761 |
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xeroderma pigmentosum, complementation group 1
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C536765 |
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complementation group 1 xeroderma pigmentosum
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C536765 |
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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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XY female 46
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C536769 |
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inferolateral myocardial infarct
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3676 |
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