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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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Isolated sternocostoclavicular hyperostosis
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Orphanet_178311 |
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Transient congenital hypothyroidism
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Orphanet_178045 |
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Acute lung injury
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Orphanet_178320 |
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Neurogenic diabetes insipidus
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Orphanet_178029 |
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Primary cutaneous marginal zone B-cell lymphoma
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Orphanet_178536 |
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Autosomal dominant non-syndromic intellectual disability
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Orphanet_178469 |
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Forsius-Eriksson type ocular albinism
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Orphanet_178333 |
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Reticulate acropigmentation of Kitamura
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Orphanet_178307 |
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Embryonal sarcoma of the liver
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Orphanet_178315 |
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Undifferentiated sarcoma of the liver
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Orphanet_178315 |
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Autosomal recessive osteopetrosis type 7
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Orphanet_178389 |
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Congenital convex pes valgus
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Orphanet_178382 |
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Rare peripheral precocious puberty
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Orphanet_178040 |
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Localized pagetoid reticulosis
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Orphanet_178517 |
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Undifferentiated embryonal sarcoma of the liver
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Orphanet_178315 |
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