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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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Conotruncal anomaly face syndrome
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Orphanet_567 |
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Idiopathic non-lupus full-house nephropathy
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Orphanet_567544 |
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Carcinoma of gallbladder and EBT
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Orphanet_56044 |
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Carcinoma of gallbladder and extrahepatic biliary tract
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Orphanet_56044 |
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Menkes kinky hair disease
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Orphanet_565 |
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Autoantibody-negative autoimmune hepatitis
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Orphanet_563589 |
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Seronegative autoimmune hepatitis
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Orphanet_563589 |
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Angiomatoid fibrous histiocytoma
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Orphanet_569164 |
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PIEZO1-related lymphatic-related hydrops fetalis
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Orphanet_568062 |
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EPHB4-related lymphatic-related hydrops fetalis
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Orphanet_568065 |
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Isolated congenital hypoglossia
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Orphanet_563954 |
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Isomerism of left atrial appendage
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Orphanet_566862 |
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Congenital primary lymphedema of Gordon
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Orphanet_569821 |
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Disorder with multisystemic involvement and glomerulopathy
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Orphanet_567562 |
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Disorder with multisystemic involvement and primary lymphedema
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Orphanet_568047 |
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