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| created at |
2021-12-20 02:12:37 UTC |
| updated at |
2021-12-22 07:05:13 UTC |
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MONDO_prefferred_names from the Bioportal site.
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24,286 entries
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There is 0 pattern entry.
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hereditary spastic paraplegia 23
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10046.0 |
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xeroderma pigmentosum group G
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10216.0 |
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autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency
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17900.0 |
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urethra adenocarcinoma
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3200.0 |
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osteosclerotic chondrodysplasia, lethal, with intracellular inclusions
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11316.0 |
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methimazole embryofetopathy
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16017.0 |
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epileptic encephalopathy, infantile or early childhood
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20627.0 |
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metachromatic leukodystrophy, adult form
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17730.0 |
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congenital genu recurvatum
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17560.0 |
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obsolete congenital fibrosis of the extraocular muscles
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869.0 |
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syndrome with a symptomatic strabismus
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20253.0 |
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immunodeficiency-associated lymphoproliferative disease
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20083.0 |
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non-invasive bladder urothelial carcinoma
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3930.0 |
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Yunis-Varon syndrome
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8995.0 |
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Bartsocas-Papas syndrome
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9901.0 |
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