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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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Athyreosis
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Orphanet_95713 |
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Acropectorovertebral dysplasia
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Orphanet_957 |
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F syndrome
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Orphanet_957 |
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X-linked AHC
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Orphanet_95702 |
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Thyroid ectopia
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Orphanet_95712 |
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Thyroid dyshormonogenesis
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Orphanet_95716 |
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Thyroid hemiagenesis
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Orphanet_95719 |
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Thyroid hypoplasia
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Orphanet_95720 |
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X-linked congenital adrenal hypoplasia
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Orphanet_95702 |
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Congenital hypothyroidism due to developmental anomaly
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Orphanet_95711 |
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Familial thyroid dyshormonogenesis
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Orphanet_95716 |
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Hypospadias, severe form
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Orphanet_95706 |
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X-linked adrenal hypoplasia congenita
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Orphanet_95702 |
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Familial adrenal hypoplasia with absent pituitary LH
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Orphanet_95700 |
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Familial adrenal hypoplasia, miniature type
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Orphanet_95700 |
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