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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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stage 0 carcinoma of oropharynx
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21298 |
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stage 0 carcinoma of the oropharynx
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21298 |
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autosomal agammaglobulinemia caused by mutation in CD79B
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12987 |
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hereditary spherocytosis caused by mutation in EPB42
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12985 |
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hypogonadotropic hypogonadism caused by mutation in FGF8
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12988 |
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cone-rod dystrophy caused by mutation in PROM1
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12983 |
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hereditary spherocytosis caused by mutation in SLC4A1
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12981 |
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SLC1A3 hereditary episodic ataxia
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12982 |
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oropharyngeal carcinoma in situ
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21298 |
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oropharynx carcinoma in situ
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21298 |
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mitral valve incompetence
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1298 |
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schizophrenia susceptibility locus, chromosome 18-Related
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http://purl.obolibrary.org/obo/MONDO_0011298 |
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FGF8 hypogonadotropic hypogonadism
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12988 |
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congenital mitral insufficiency
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1298 |
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mitral valve insufficiency
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1298 |
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