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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.
primary thymic epithelial neoplasm
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6456 |
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primary thymic epithelial tumor
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6456 |
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infantile liver failure syndrome type 1
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24568 |
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glaucoma iridogoniodysplasia, familial
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24456 |
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tumor of follicular infundibulum
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4560 |
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progressive, and hypogonadotropic hypogonadism adrenal insufficiency
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C564568 |
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acute leukemia, hybrid
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D015456 |
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acute leukemias, hybrid
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D015456 |
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short-chain enoyl-CoA hydratase deficiency
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14563 |
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basal cell hamartoma with follicular differentiation
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4560 |
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amelogenesis imperfecta, hypoplastic type 1F
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14560 |
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amelogenesis imperfecta hypoplastic type IF
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14560 |
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postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome
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14567 |
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apocrine carcinoma in situ of breast
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4562 |
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apocrine carcinoma in situ of the breast
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4562 |
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