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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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Congenital isolated growth hormone deficiency type III
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Orphanet_231692 |
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Isolated growth hormone deficiency type IA
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Orphanet_231662 |
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Isolated growth hormone deficiency type IB
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Orphanet_231671 |
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Isolated growth hormone deficiency type II
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Orphanet_231679 |
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Isolated growth hormone deficiency type III
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Orphanet_231692 |
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Alopecia-anosmia-conductive hearing loss-hypogonadism syndrome
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Orphanet_2316 |
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Rare non surgically correctable form of primary aldosteronism
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Orphanet_231641 |
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Johnson neuroectodermal syndrome
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Orphanet_2316 |
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Ectopic aldosterone-producing tumor
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Orphanet_231632 |
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Extra-adrenal aldosterone-producing tumor
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Orphanet_231632 |
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Congenital IGHD type IA
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Orphanet_231662 |
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Congenital IGHD type IB
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Orphanet_231671 |
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Congenital IGHD type II
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Orphanet_231679 |
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Congenital IGHD type III
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Orphanet_231692 |
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Adrenocortical carcinoma with pure aldosterone hypersecretion
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Orphanet_231625 |
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