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| created at |
2021-12-23 02:14:06 UTC |
| updated at |
2021-12-23 14:43:01 UTC |
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"MeSH2022Disease.tsv"
"MeSH2022MentalDisorder.tsv"
"Addition_for_LitCoin_Disease_2.tsv"
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82,725 entries
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There is 0 pattern entry.
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phenylketonuria type 2
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D010661 |
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deficiency, phenylalanine hydroxylase
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D010661 |
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dihydropteridine reductase deficiency
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D010661 |
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phenylalanine hydroxylase deficiency
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D010661 |
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dihydropteridine reductase deficiency disease
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D010661 |
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phenylalanine hydroxylase deficiency disease
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D010661 |
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phenylalanine hydroxylase deficiency disease, severe
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D010661 |
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hyperphenylalaninemia caused by a defect in biopterin metabolism
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D010661 |
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hyperphenylalaninemia, BH4-Deficient, c
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D010661 |
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hyperphenylalaninemia, tetrahydrobiopterin-deficient, due to DHPR deficiency
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D010661 |
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deficiency disease, dihydropteridine reductase
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D010661 |
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severe phenylalanine hydroxylase deficiency disease
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D010661 |
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BH4-Deficient, c hyperphenylalaninemia
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D010661 |
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non phenylketonuric hyperphenylalaninemia
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D010661 |
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tetrahydrobiopterin-deficient, due to DHPR deficiency hyperphenylalaninemia
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D010661 |
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