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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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syndromes, post-lyme disease
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D000077342 |
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inborn genetic disease
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D030342 |
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mandibulofacial (MFD1) dysostoses
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D008342 |
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mandibulofacial (MFD1) dysostosis
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D008342 |
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pubic bone dysplasia
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8342 |
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congenital talipes equinovarus
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7342 |
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classic complement early component deficiency caused by mutation in C8A
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13422 |
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classic complement early component deficiency caused by mutation in C8B
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13421 |
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disease, inborn genetic
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D030342 |
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treacher collins franceschetti syndrome
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D008342 |
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diseases, inborn genetic
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D030342 |
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obsolete osteoclast-like giant cell neoplasm of the pancreas
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4342.0 |
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functioning pituitary gland adenoma
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3429 |
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infection of gastrointestinal tract
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43424 |
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secretory pituitary gland adenoma
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3429 |
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