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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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intellectual disability, autosomal recessive type 34
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13785 |
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mental retardation, autosomal recessive type 34
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13785 |
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NADH cytochrome b5 reductase deficiency
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C537841 |
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dermoid cyst, benign
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2378 |
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neutral 17 beta-hydroxysteroid oxidoreductase deficiency
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C537805 |
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familial nuchal bleb
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C537852 |
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recurrent wheezy bronchitis
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3781 |
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inflammation of bronchus
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3781 |
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dental pulp calcifications
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D003784 |
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nasal cavity carcinoma in situ
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3784 |
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testicular embryonal carcinoma of childhood
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3788 |
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hereditary papillary carcinoma of kidney
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3789 |
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stage 0 carcinoma of nasal cavity
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3784 |
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childhood embryonal carcinoma of testis
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3788 |
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pediatric embryonal carcinoma of testis
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3788 |
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