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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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Hyalinosis cutis et mucosae
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Orphanet_530 |
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Autosomal recessive extra-oral halitosis
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Orphanet_562538 |
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EBS without extracutaneous involvement
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Orphanet_595346 |
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EBS with extracutaneous involvement
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Orphanet_595351 |
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Congenital cystic eye
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Orphanet_519384 |
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Structural developmental eye defect
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Orphanet_519272 |
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Structural developmental eye defect of genetic origin
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Orphanet_522536 |
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Rare genetic eyelid malposition disorder
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Orphanet_522528 |
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Conotruncal anomaly face syndrome
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Orphanet_567 |
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Infantile-onset periodic fever-panniculitis-dermatosis syndrome
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Orphanet_500062 |
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Incomplete septal fibrosis
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Orphanet_596941 |
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Myxoma with fibrous dysplasia
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Orphanet_57782 |
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Lichen planus follicularis
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Orphanet_525 |
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Idiopathic non-lupus full-house nephropathy
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Orphanet_567544 |
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Sorsby pseudoinflammatory fundus dystrophy
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Orphanet_59181 |
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