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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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Grange syndrome
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Orphanet_79094 |
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AMACR deficiency
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Orphanet_79095 |
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PNPO deficiency
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Orphanet_79096 |
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Sympathetic ophthalmia
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Orphanet_79098 |
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Sympathetic uveitis
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Orphanet_79098 |
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Ackerman syndrome
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Orphanet_79099 |
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Congenital bile acid synthesis defect type 4
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Orphanet_79095 |
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Disorder of amino acid and other organic acid metabolism
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Orphanet_79062 |
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Chronic dacryoadenitis and sialadenitis
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Orphanet_79078 |
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IgG4-related dacryoadenitis and sialadenitis
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Orphanet_79078 |
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Grange occlusive arterial syndrome
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Orphanet_79094 |
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Hereditary inclusion body myopathy type 3
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Orphanet_79091 |
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2-methylacyl-CoA racemase deficiency
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Orphanet_79095 |
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Alpha-methyl-acyl-CoA racemase deficiency
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Orphanet_79095 |
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Pyridoxamine 5'-oxidase deficiency
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Orphanet_79096 |
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