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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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polydactyly with neonatal chondrodystrophy type II
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9894 |
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polydactyly with neonatal chondrodystrophy, type 2
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9894 |
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polydactyly with neonatal chondrodystrophy, type II
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9894 |
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HEREDITARY PERSISTENCE of FETAL HEMOGLOBIN
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20989 |
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Hereditary Persistence of Fetal Hemoglobin
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20989 |
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hereditary persistence of fetal hemoglobin
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20989 |
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polysaccharide, storage of unusual
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9898 |
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pes disease or disorder
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44989 |
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atypical MRKH syndrome
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10989 |
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suppurative apical periodontitis
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6989 |
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suppurative periapical periodontitis
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6989 |
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disease of pes
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44989 |
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disorder of pes
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44989 |
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recurrent acute pancreatitis
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18989 |
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autosomal recessive primary microcephaly caused by mutation in STIL
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12989 |
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