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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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partial monosomy of the short arm of chromosome 12
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17848 |
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partial deletion of the short arm of chromosome type 12
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17848 |
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nonmedullary, with or without cell oxyphilia thyroid carcinoma
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C537842 |
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cytochrome c oxidase deficiency, fatal infantile, with cardioencephalomyopathy
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C565784 |
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autosomal recessive parkinson disease 14
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C567844 |
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multiple sclerosis, pediatric
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18784 |
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preaxial III polydactyly
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C566784 |
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familial amyloid polyneuropathy type iv
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C000657784 |
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humeral fracture, proximal
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D012784 |
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humeral fractures, proximal
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D012784 |
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calcification, dental pulp
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D003784 |
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calcifications, dental pulp
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D003784 |
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stone, dental pulp
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D003784 |
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stones, dental pulp
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D003784 |
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integument hypersensitivity reaction type II disease
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17841 |
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