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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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episodic ataxia type 4
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11681.0 |
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transient tyrosinemia of the newborn
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18083.0 |
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dilated cardiomyopathy 1M
|
11840.0 |
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intellectual disability-facial dysmorphism-hand anomalies syndrome
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18253.0 |
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Stargardt disease
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19353.0 |
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short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome
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11227.0 |
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HPC15
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12770.0 |
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spermatogenic failure 6
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7060.0 |
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trisomy 10p
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15761.0 |
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limbic encephalitis associated with antibodies to cell membrane antigens
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15591.0 |
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Schaap-Taylor-Baraitser syndrome
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42908.0 |
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cerebrovascular disorder
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11057.0 |
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Pierre Robin syndrome associated with collagen disease
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15318.0 |
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congenital myasthenic syndrome 4C
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12157.0 |
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autosomal recessive nonsyndromic deafness 46
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12327.0 |
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