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Deficiency Disease, Hexosaminidase A and B - C0036161 L1401060 S1669017 A1631084 M0019413 MeSH EN D012497 → |
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Deficiency Disease, Hypoxanthine Phosphoribosyl Transferase - C0023374 L1406740 S1681190 A1642681 M0012368 MeSH PM D007926 → |
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Deficiency Disease, Hypoxanthine-Phosphoribosyl-Transferase - C0023374 L1406740 S1681191 A1642682 M0012368 MeSH EN D007926 → |
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Deficiency Disease, Lysosomal alpha-1,4-Glucosidase - C0017921 L1395700 S1662639 A1624841 M0009470 MeSH EN D006009 → |
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Deficiency Disease, Ornithine Carbamoyltransferase (MeSH) - C0268542 L1404891 S1677333 A1639021 M0328321 MeSH EN D020163 → |
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Deficiency Disease, Ornithine Transcarbamylase (MeSH) - C0268542 L1406743 S1681202 A1642693 M0328321 MeSH EN D020163 → |
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Deficiency Disease, PDHC - C0034345 L1406744 S1681204 A1642695 M0023594 MeSH PM D015325 → |
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Deficiency Disease, Pyruvate Carboxylase - C0034341 L1404909 S1677353 A1639042 M0023593 MeSH EN D015324 → |
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Deficiency Disease, Tyrosine Transaminase (MeSH) - C0268487 L1406746 S1681216 A1642705 M0336267 MeSH EN D020176 → |
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Deficiency Diseases - C0011156 L0011156 S0030524 A0045860 M0005753 MeSH MH D003677 → |
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