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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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X-linked non-syndromic sensorineural hearing loss type DFN
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Orphanet_90625 |
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Moderate and severe traumatic brain injury
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Orphanet_90056 |
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Difference of sex development
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Orphanet_90771 |
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Disorder of sex development
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Orphanet_90771 |
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Hereditary hypotrichosis simplex of the scalp
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Orphanet_90368 |
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Other acquired skin disease
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Orphanet_90077 |
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Acquired aneurysmal subarachnoid hemorrhage
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Orphanet_90065 |
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AIDS wasting syndrome
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Orphanet_90081 |
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CMT-deafness-intellectual disability syndrome
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Orphanet_90103 |
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Parkes Weber syndrome
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Orphanet_90307 |
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Brittle cornea syndrome
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Orphanet_90354 |
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Hearing loss-hypogonadism syndrome
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Orphanet_90646 |
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OPD I syndrome
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Orphanet_90650 |
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OPD II syndrome
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Orphanet_90652 |
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Charcot-Marie-Tooth disease-deafness syndrome
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Orphanet_90658 |
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