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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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Prader-Willi syndrome due to maternal uniparental disomy of chromosome type 15
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20298 |
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chromosome 17q21.31 duplication syndrome
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13298 |
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PROM1 cone-rod dystrophy
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12983 |
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syndromes, neuroectodermal dysplasia
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42983 |
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alzheimer disease, familial, 1
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C566298 |
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cerebellar ataxia early-onset nonprogressive
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7298 |
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autosomal recessive, early-onset, pulverulent cataract
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C565298 |
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SLC1A3 hereditary episodic ataxia
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12982 |
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mammalian vulva leiomyoma
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3298 |
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isolated postlingual genetic deafness
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16298 |
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postlingual non-syndromic genetic deafness
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16298 |
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malignant mediastinal germ cell neoplasm
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6298 |
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malignant mediastinal germ cell tumor
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6298 |
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mediastinal malignant germ cell tumor
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6298 |
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thymic malignant germ cell tumor
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6298 |
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