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| created at |
2024-09-23 16:23:50 UTC |
| updated at |
2024-09-23 18:22:39 UTC |
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Terms for rare diseases as defined in ORDO.
The entries were initially sourced from the ORDO version 2024-07-03 as stored in BioPortal.
Namespace: http://www.orpha.net/ORDO/
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20,514 entries
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There is 0 pattern entry.
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GSDIb
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Orphanet_79259 |
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G6PT deficiency
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Orphanet_79259 |
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GSD type 1 non a
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Orphanet_79259 |
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GSD type 1b
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Orphanet_79259 |
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Glycogenosis type 1b
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Orphanet_79259 |
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GSD type Ib
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Orphanet_79259 |
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Glycogenosis type Ib
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Orphanet_79259 |
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G6P translocase deficiency
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Orphanet_79259 |
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Glycogen storage disease due to G6P deficiency type Ib
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Orphanet_79259 |
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Glycogen storage disease type 1b
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Orphanet_79259 |
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Glycogen storage disease type Ib
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Orphanet_79259 |
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GSD due to G6P deficiency type 1b
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Orphanet_79259 |
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GSD due to G6P deficiency type Ib
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Orphanet_79259 |
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GSD due to G6PT deficiency
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Orphanet_79259 |
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Glycogenosis due to glucose-6-phosphatase deficiency type 1b
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Orphanet_79259 |
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