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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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unilateral polymicrogyria
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17092 |
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deficiency of uroporphyrinogen III synthase
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D017092 |
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erythropoietic porphyria, congenital
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D017092 |
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erythropoietic porphyrias, congenital
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D017092 |
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porphyria, erythropoietic, congenital
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D017092 |
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erythropoietic, congenital porphyria
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D017092 |
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congenital erythropoietic porphyrias
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D017092 |
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Gunther's disease
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D017092 |
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UROS deficiency
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D017092 |
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erythropoietic porphyrias
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D017092 |
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gunther disease
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D017092 |
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gunthers disease
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D017092 |
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porphyria, erythropoietic
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D017092 |
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porphyrias, erythropoietic
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D017092 |
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porphyrias, congenital erythropoietic
|
D017092 |
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