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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.
COXPD29
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Orphanet_478029 |
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COXPD30
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Orphanet_478042 |
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HSAN8
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Orphanet_478664 |
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Kallmann syndrome
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Orphanet_478 |
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Hereditary sensory and autonomic neuropathy type 8
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Orphanet_478664 |
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Hereditary sensory and autonomic neuropathy type VIII
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Orphanet_478664 |
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Congenital hypogonadotropic hypogonadism with anosmia
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Orphanet_478 |
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Combined oxidative phosphorylation defect type 29
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Orphanet_478029 |
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Combined oxidative phosphorylation defect type 30
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Orphanet_478042 |
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Olfacto-genital pathological sequence
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Orphanet_478 |
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