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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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opalescent dentin, hereditary
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D003811 |
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visceral, X-linked heterotaxy
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C538116 |
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neuroblastoma with hirschsprung disease
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C538119 |
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benign prostate hyperplasia
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10811 |
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benign prostatic hyperplasia
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10811 |
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benign prostatic hyperplasia (disease)
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10811 |
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benign prostatic hyperplasia - BPH
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10811 |
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benign prostatic hypertrophy
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10811 |
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cleft palate, hypotelorism, and hypospadias
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8113 |
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severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion
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17811 |
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disorder, gender identity
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D000068116 |
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loa loa infection
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D008118 |
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microcephaly-digital anomalies-normal intelligence syndrome type 1
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8115 |
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neoplasms, experimental liver
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D008114 |
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filariasis, loa loa
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D008118 |
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