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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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Transient erythroblastopenia of childhood
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Orphanet_98871 |
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Gonadal dysgenesis of gynecological interest
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Orphanet_98074 |
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46,XY difference of sex development
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Orphanet_98085 |
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46,XY disorder of sex development
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Orphanet_98085 |
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46,XX difference of sex development induced by androgens excess
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Orphanet_98078 |
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46,XX disorder of sex development induced by androgens excess
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Orphanet_98078 |
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Subepithelial amyloidosis of the cornea
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Orphanet_98957 |
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Developmental defect of the eye
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Orphanet_98553 |
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Congenital malformation of the eyelid
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Orphanet_98561 |
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Congenital anomaly of the great arteries
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Orphanet_98724 |
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Rare disorder of the lacrimal apparatus
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Orphanet_98602 |
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Excretory apparatus of the lacrimal system anomaly
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Orphanet_98605 |
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Infectious disease of the nervous system
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Orphanet_98010 |
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Azorean disease of the nervous system
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Orphanet_98757 |
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Congenital absence of the pulmonary valve
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Orphanet_982 |
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