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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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ACHM
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Orphanet_49382 |
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Achromatopsia
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Orphanet_49382 |
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Familial keratoacanthoma
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Orphanet_493 |
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Hereditary keratoacanthoma
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Orphanet_493 |
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Multiple keratoacanthoma
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Orphanet_493 |
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Vibratory angioedema/urticaria
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Orphanet_493342 |
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Vibratory urticaria
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Orphanet_493342 |
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Pingelapese blindness
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Orphanet_49382 |
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Rod monochromacy
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Orphanet_49382 |
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Rod monochromatism
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Orphanet_49382 |
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Total color blindness
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Orphanet_49382 |
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Complete or incomplete color blindness
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Orphanet_49382 |
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