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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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Lenz microphthalmia
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Orphanet_568 |
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WILD syndrome
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Orphanet_568056 |
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PIEZO1-related LRHF/GLD
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Orphanet_568062 |
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EPHB4-related LRHF/GLD
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Orphanet_568065 |
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Generalized lymphatic dysplasia of Fotiou
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Orphanet_568062 |
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PIEZO1-related lymphatic-related hydrops fetalis
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Orphanet_568062 |
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EPHB4-related lymphatic-related hydrops fetalis
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Orphanet_568065 |
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Disorder with multisystemic involvement and primary lymphedema
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Orphanet_568047 |
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GJC2-related late-onset primary lymphedema
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Orphanet_568051 |
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Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome
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Orphanet_568056 |
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Microphthalmia, Lenz type
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Orphanet_568 |
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Primary lymphedema with systemic or visceral involvement
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Orphanet_568044 |
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Primary lymphedema without systemic or visceral involvement
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Orphanet_568041 |
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