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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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type 1 diabetes mellitus caused by mutation in CCR5
|
12921 |
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paternal uniparental disomy of chromosome 6
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19921 |
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obsolete inborn disorder of urea cycle metabolism and ammonia detoxification
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19217.0 |
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glycogen storage disease 11
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9216 |
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glycogen storage disease due to GLUT2 deficiency
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9216 |
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paternal uniparental disomy of chromosome type 6
|
19921 |
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carbohydrate metabolic disorder
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19214 |
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carbohydrate metabolism disorder
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19214 |
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atypical lymphoproliferative disorder
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44921 |
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actinomycetales caused disease or disorder
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6921 |
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Actinomycetales caused disease or disorder
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http://purl.obolibrary.org/obo/MONDO_0006921 |
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sleep arousal disorder
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D020921 |
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glycogen storage disease type XI
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9216 |
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sleep arousal disorders
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D020921 |
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traumatic stress disorders
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D040921 |
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