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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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Alopecia-anosmia-deafness-hypogonadism syndrome
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Orphanet_2316 |
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Johnson-McMillin syndrome
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Orphanet_2316 |
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Pure APAC
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Orphanet_231625 |
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X-linked IGHD
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Orphanet_231692 |
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Congenital isolated GH deficiency type IA
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Orphanet_231662 |
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Congenital isolated GH deficiency type IB
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Orphanet_231671 |
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Congenital isolated GH deficiency type II
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Orphanet_231679 |
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Congenital isolated GH deficiency type III
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Orphanet_231692 |
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Pure aldosterone-producing adrenocortical carcinoma
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Orphanet_231625 |
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Pure aldosterone-secreting adrenocortical carcinoma
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Orphanet_231625 |
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Rare surgically correctable form of primary aldosteronism
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Orphanet_231637 |
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X-linked isolated growth hormone deficiency
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Orphanet_231692 |
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Congenital isolated growth hormone deficiency type IA
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Orphanet_231662 |
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Congenital isolated growth hormone deficiency type IB
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Orphanet_231671 |
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Congenital isolated growth hormone deficiency type II
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Orphanet_231679 |
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