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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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Deafness with labyrinthine aplasia, microtia, and microdontia
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Orphanet_90024 |
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Congenital folate malabsorption
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Orphanet_90045 |
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Hereditary folate malabsorption
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Orphanet_90045 |
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Microdontia-type I microtia-deafness syndrome
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Orphanet_90024 |
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Microdontia-type I microtia-hearing loss syndrome
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Orphanet_90024 |
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Parkinson-dementia complex of Guam
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Orphanet_90020 |
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Inflammatory pseudotumor of the liver
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Orphanet_90003 |
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Systemic monochloroacetate poisoning
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Orphanet_90069 |
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Granulomatosis with polyangiitis
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Orphanet_900 |
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Primary familial polycythemia
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Orphanet_90042 |
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Sepsis in premature infants
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Orphanet_90051 |
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Retinopathy of prematurity
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Orphanet_90050 |
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Hepatitis B reinfection following liver transplantation
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Orphanet_90073 |
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Secondary acute sensorineural hearing loss
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Orphanet_90059 |
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Moderate and severe traumatic brain injury
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Orphanet_90056 |
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