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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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hereditary papillary carcinoma of the kidney
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3789 |
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cone-rod dystrophy caused by mutation in C8orf37
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13786 |
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stage 0 carcinoma of the nasal cavity
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3784 |
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childhood embryonal carcinoma of the testis
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3788 |
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pediatric embryonal carcinoma of the testis
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3788 |
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White blood cell decreased
|
3785 |
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Usher syndrome caused by mutation in HARS
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13788 |
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retinitis pigmentosa caused by mutation in RP9
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8378 |
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orofacial cleft caused by mutation in SUMO1
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13378 |
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Noonan-like-multiple giant cell lesion syndrome
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C537846 |
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malignant Sertoli cell tumor
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378 |
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nonseminomatous germ cell tumor
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C537844 |
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disorder of cellular amino acid metabolic process
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37871 |
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monosomy 6q chromosome 6
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C537807 |
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CI - chest infection
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3781 |
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