glycogen storage disease
(Q1421738)
glycogen metabolism disorder that has material basis in enzymes deficiencies necessary in the processing of glycogen synthesis or breakdown within muscles, liver, and other cell types
glycogen metabolism disorder that has material basis in enzymes deficiencies necessary in the processing of glycogen synthesis or breakdown within muscles, liver, and other cell types
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Current Data About
glycogen storage disease
| (P18) |
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| (P31) |
(Q112193867)
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| (P279) |
(Q18553432)
(Q1496114) (Q6013981) (Q12136) |
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| (P373) |
Glycogen storage disease
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| (P910) |
(Q9501412)
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| (P1692) |
271.0
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| (P1748) |
C61272
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| (P1995) |
(Q162606)
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| (P2176) |
(Q2919537)
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| (P2293) |
(Q17815968)
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_2747
http://identifiers.org/doid/DOID:2747
http://www.orpha.net/ORDO/Orphanet_79201 |
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| (P5008) |
(Q4099686)
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other details
| aliases |
glycogenosis dextrinosis GSD glycogenoses |
| description | glycogen metabolism disorder that has material basis in enzymes deficiencies necessary in the processing of glycogen synthesis or breakdown within muscles, liver, and other cell types |
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