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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.
Primary early-onset glaucoma
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Orphanet_156005 |
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Genetic endocrine growth disease
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Orphanet_156643 |
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Beare-Stevenson cutis gyrata syndrome
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Orphanet_1555 |
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Symbrachydactyly of hands and feet
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Orphanet_1570 |
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Rare genetic hematologic disease
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Orphanet_158300 |
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Rare genetic hepatic disease
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Orphanet_156601 |
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Generalized eruptive histiocytoma
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Orphanet_157991 |
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Non-Langerhans cell histiocytosis
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Orphanet_157987 |
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Generalized eruptive histiocytosis
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Orphanet_157991 |
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Benign cephalic histiocytosis
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Orphanet_157997 |
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Indeterminate cell histiocytosis
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Orphanet_158019 |
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Progressive nodular histiocytosis
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Orphanet_158022 |
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Familial benign hypocupremia
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Orphanet_1551 |
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Familial or idiopathic dilated cardiomyopathy
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Orphanet_154 |
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Common variable immunodeficiency
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Orphanet_1572 |
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