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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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Atrial auricle anomaly
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Orphanet_95510 |
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Primary progressive aphasia
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Orphanet_95432 |
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Pituitary tumor apoplexy
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Orphanet_95613 |
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Patent ductus arteriosus anomalies
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Orphanet_95485 |
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Congenital coronary artery aneurysm
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Orphanet_95491 |
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Secondary short bowel syndrome
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Orphanet_95427 |
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Autosomal recessive cerebellar ataxia-movement disorder syndrome
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Orphanet_95434 |
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Post-traumatic pituitary deficiency
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Orphanet_95619 |
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Pituitary hormone deficiency of meningeal origin
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Orphanet_95505 |
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Pituitary hormone deficiency of tumoral origin
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Orphanet_95503 |
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Pituitary hormone deficiency of vascular origin
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Orphanet_95611 |
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Pituitary hormone deficiency secondary to storage disease
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Orphanet_95618 |
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Acquired neurogenic diabetes insipidus
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Orphanet_95626 |
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Congenital hypothyroidism due to developmental anomaly
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Orphanet_95711 |
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Familial thyroid dyshormonogenesis
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Orphanet_95716 |
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