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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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Rare genetic disorder of the anterior segment of the eye
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Orphanet_522538 |
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Rare genetic disorder of the lacrimal apparatus
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Orphanet_522532 |
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Rare genetic disorder of the ocular adnexa
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Orphanet_522524 |
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Rare genetic disorder of the posterior segment of the eye
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Orphanet_522570 |
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Rare genetic disorder of the pupil
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Orphanet_522568 |
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Rare genetic disorder of the visual organs
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Orphanet_522504 |
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Rare ophthalmic disorder with cortical involvement
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Orphanet_519343 |
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Rare ophthalmic disorder with cranial nerve involvement
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Orphanet_519349 |
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Rare genetic disorder with entropion
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Orphanet_522530 |
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Rare genetic disorder with lens opacification
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Orphanet_522546 |
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Rare genetic disorder with strabismus
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Orphanet_522518 |
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Syndromic genetic disorder with strabismus
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Orphanet_522520 |
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group of disorders
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Orphanet_557492 |
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Laing early-onset distal myopathy
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Orphanet_59135 |
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Osteopetrosis autosomal dominant type 2
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Orphanet_53 |
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