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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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disorder of amino acid absorption and transport
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19216 |
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disorder of amino acid transport
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19216 |
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GSD type XI
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9216 |
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glycogen storage disease type XI
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9216 |
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glycogen storage disease 11
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9216 |
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Fanconi Bickel syndrome
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9216 |
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inborn disorder of amino acid absorption and transport
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19216 |
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fear of the moon
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C000719216 |
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hepatic glycogenosis with Fanconi nephropathy
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9216 |
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glycogenosis, Fanconi type
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9216 |
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GSD due to GLUT2 deficiency
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9216 |
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glycogenosis due to GLUT2 deficiency
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9216 |
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hepatic glycogenosis with amino aciduria and glucosuria
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9216 |
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Fanconi syndrome with intestinal malabsorption and galactose intolerance
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9216 |
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hepatorenal glycogenosis with renal Fanconi syndrome
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9216 |
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