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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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FCMD
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Orphanet_272 |
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OODD
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Orphanet_2721 |
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Odonto-onycho-dermal dysplasia
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Orphanet_2721 |
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Freire-Maia syndrome
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Orphanet_2723 |
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Odontotrichomelic syndrome
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Orphanet_2723 |
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Boder syndrome
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Orphanet_2724 |
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Ohdo syndrome
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Orphanet_2728 |
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Ohdo-Madokoro-Sonoda syndrome
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Orphanet_2728 |
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Blepharophimosis syndrome, Ohdo type
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Orphanet_2728 |
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Congenital muscular dystrophy, Fukuyama type
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Orphanet_272 |
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FKTN-related congenital muscular dystrophy
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Orphanet_272 |
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Fukuyama congenital muscular dystrophy
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Orphanet_272 |
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Odontomatosis-aortae esophagus stenosis syndrome
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Orphanet_2724 |
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Odonto-onycho dysplasia-alopecia syndrome
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Orphanet_2722 |
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Blepharophimosis-intellectual disability syndrome, Ohdo type
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Orphanet_2728 |
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