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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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Syndrome with a symptomatic strabismus
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Orphanet_98683 |
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Diaphragmatic or abdominal wall malformation
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Orphanet_98043 |
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Internal carotid absence
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Orphanet_981 |
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Minimally differentiated acute myeloblastic leukemia
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Orphanet_98832 |
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Pulmonary valve agenesis
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Orphanet_982 |
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XY gonadal agenesis syndrome
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Orphanet_983 |
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Rare respiratory allergy
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Orphanet_98052 |
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Primary familial amyloidosis of the cornea
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Orphanet_98957 |
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CD30 positive anaplastic large cell lymphoma
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Orphanet_98841 |
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Ki-1 positive anaplastic large cell lymphoma
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Orphanet_98841 |
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Noonan syndrome and Noonan-related syndrome
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Orphanet_98733 |
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Rare hyperopia and astigmatism
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Orphanet_98621 |
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Atrial defect and interauricular communication
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Orphanet_98727 |
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Cranial nerve and nuclear aplasia
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Orphanet_98518 |
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EEC syndrome and related disorders
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Orphanet_98609 |
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