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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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arrhythmogenic right ventricular dysplasia 11
|
12506.0 |
|
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obsolete polymicrogyria
|
18176.0 |
|
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ferro-cerebro-cutaneous syndrome
|
18346.0 |
|
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localized lichen myxedematosus
|
19446.0 |
|
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inherited epidermolysis bullosa
|
19276.0 |
|
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variable age onset epilepsy
|
100036.0 |
|
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hypertrophic cardiomyopathy 19
|
13476.0 |
|
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cardiocranial syndrome, Pfeiffer type
|
9036.0 |
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gnathomiasis
|
5776.0 |
|
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generalized basal epidermolysis bullosa simplex with skin atrophy, scarring and hair loss
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15006.0 |
|
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progressive muscular dystrophy
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16106.0 |
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familial thyroid dyshormonogenesis 1
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20716.0 |
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thyroid dyshormonogenesis 4
|
10136.0 |
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X-linked intellectual disability, Cabezas type
|
10306.0 |
|
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hyperinsulinism due to glucokinase deficiency
|
11236.0 |
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