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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.
hereditary thrombophilia due to congenital HRG deficiency
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13143 |
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hereditary thrombophilia due to congenital antithrombin 3 deficiency
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13144 |
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hereditary thrombophilia due to congenital antithrombin deficiency
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13144 |
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hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
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13143 |
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malignant cutaneous granular cell skin tumor
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4314 |
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malignant cutaneous granular cell tumor
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4314 |
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fish tank granuloma
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43314 |
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swimming pool granuloma
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43314 |
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fetal brain disruption sequence
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23142 |
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TUBB1 autosomal dominant macrothrombocytopenia
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13141 |
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emery-dreifuss, autosomal dominant muscular dystrophy
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D000083144 |
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hauptmann-thannhauser muscular dystrophy
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D000083144 |
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emery-dreifuss muscular dystrophy 1
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D000083143 |
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emery-dreifuss muscular dystrophy 1, x-linked
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D000083143 |
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emery-dreifuss muscular dystrophy 2
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D000083144 |
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