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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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Subcortical band heterotopia
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Orphanet_99796 |
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Subcortical laminar heterotopia
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Orphanet_99796 |
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Pulmonary artery hypoplasia
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Orphanet_99083 |
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Familial isolated hyperparathyroidism
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Orphanet_99879 |
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Cow's milk hypersensitivity
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Orphanet_99932 |
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Familial gestational hyperthyroidism
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Orphanet_99819 |
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Dengue virus infection
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Orphanet_99828 |
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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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Benign recurrent intrahepatic cholestasis type 1
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Orphanet_99960 |
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Benign recurrent intrahepatic cholestasis type 2
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Orphanet_99961 |
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Infantile and juvenile forms of acromegaly
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Orphanet_99725 |
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Acute megakaryoblastic leukemia in children with Down syndrome
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Orphanet_99887 |
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Acute megakaryoblastic leukemia in children with trisomy 21
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Orphanet_99887 |
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Myxoid/round cell liposarcoma
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Orphanet_99967 |
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