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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.
obsessive compulsive disorder
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8114 |
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gender identity disorders
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D000068116 |
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ATXN1 autosomal dominant cerebellar ataxia type I
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8119 |
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ovarian mixed epithelial neoplasm
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3811 |
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ovarian mixed epithelial tumor
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3811 |
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liver neoplasm, experimental
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D008114 |
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microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1
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8115 |
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ichthyosis cheek eyebrow syndrome
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7811 |
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liver neoplasms, experimental
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D008114 |
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type 3 generalized epilepsy with febrile seizures plus
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C565811 |
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cleft palate, hypotelorism, and hypospadias
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8113 |
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renal tubulopathy-encephalopathy-liver failure syndrome
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16811 |
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opalescent dentin, hereditary
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D003811 |
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hirschsprung disease ganglioneuroblastoma
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C538119 |
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identity disorder, gender
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D000068116 |
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