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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.
Palmoplantar and periorificial keratoderma
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Orphanet_659 |
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Primary benign peritoneal tumor
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Orphanet_676030 |
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Foramina parietalia permagna
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Orphanet_60015 |
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Non-syndromic congenital phagocyte functional defect
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Orphanet_674896 |
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Isolated primary pigmented nodular adrenocortical disease
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Orphanet_647772 |
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Abnormally invasive placenta
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Orphanet_662721 |
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Isolated frontal plagiocephaly
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Orphanet_620102 |
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Isolated occipital plagiocephaly
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Orphanet_620113 |
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Parkinsonism with polyneuropathy
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Orphanet_611237 |
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Hepatic cutaneous porphyria
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Orphanet_659698 |
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Familial multiple port-wine stains
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Orphanet_624 |
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Rare central precocious puberty
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Orphanet_650063 |
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Genetic central precocious puberty
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Orphanet_650182 |
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Primary central precocious puberty in boy
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Orphanet_650087 |
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Secondary central precocious puberty in boy
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Orphanet_650092 |
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