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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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Paramacular albinotic spot syndrome
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Orphanet_674935 |
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Non-syndromic unilateral squamosal suture synostosis
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Orphanet_620146 |
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Multiple self-healing squamous epithelioma
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Orphanet_65748 |
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Ocular surface squamous neoplasia
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Orphanet_659744 |
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Dysraphism with stalk
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Orphanet_645193 |
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Congenital esophageal stenosis
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Orphanet_645749 |
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Congenital oesophageal stenosis
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Orphanet_645749 |
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Idiopathic subglottic stenosis
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Orphanet_652681 |
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Familial idiopathic steroid-resistant nephrotic syndrome
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Orphanet_656 |
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Isolated angioid streaks
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Orphanet_674943 |
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Diffuse unilateral subacute neuroretinitis
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Orphanet_674947 |
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Atlantoaxial non-traumatic subluxation
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Orphanet_662255 |
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Rare maxillo-facial surgical disease
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Orphanet_68329 |
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Non-syndromic single suture synostosis
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Orphanet_620096 |
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Non-syndromic multiple suture synostosis
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Orphanet_620152 |
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