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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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Familial gestational hyperthyroidism
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Orphanet_99819 |
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Myxoid/round cell liposarcoma
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Orphanet_99967 |
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Dengue virus infection
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Orphanet_99828 |
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Mesial temporal lobe epilepsy with hippocampal sclerosis
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Orphanet_99701 |
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Bird fancier lung
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Orphanet_99908 |
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Adult-onset vitelliform macular dystrophy
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Orphanet_99000 |
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Butterfly-shaped pigmentary macular dystrophy
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Orphanet_99001 |
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DS-AMKL in children with Down syndrome
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Orphanet_99887 |
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DS-AMKL in children with trisomy 21
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Orphanet_99887 |
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Mosaic trisomy chromosome 9
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Orphanet_99776 |
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Primary thymic epithelial neoplasm
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Orphanet_99867 |
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Primary thymic epithelial tumor
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Orphanet_99867 |
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Absence of innominate vein
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Orphanet_99112 |
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Complete androgen insensitivity syndrome
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Orphanet_99429 |
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Granulosa cell malignant tumor
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Orphanet_99915 |
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