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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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persistent mullerian duct syndrome, types i and II
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C536665 |
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X-linked acrogigantism due to a point mutation
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18665 |
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monostotic fibrous dysplasia
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19665 |
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monostotic fibrous dysplasia (disease)
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19665 |
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lethal skeletal dysplasia and progressive central nervous system degeneration
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C566514 |
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monostotic fibrous dysplasia of bone
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19665 |
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primary cervical dystonia
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C566572 |
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leukoencephalopathy with dystonia and motor neuropathy, SCPx-Deficient
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C566654 |
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complementation group e peroxisome biogenesis disorder
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C566569 |
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cervix uteri endometrioid adenocarcinoma
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3665 |
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uterine cervix endometrioid adenocarcinoma
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3665 |
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cervix uteri endometrioid carcinoma
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3665 |
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uterine cervix endometrioid carcinoma
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3665 |
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retinal pigment epithelium lesions, discolored teeth sensorineural hearing loss
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C566560 |
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apparent mineralocorticoid excess syndrome
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6657 |
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