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| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
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MONDO_bioport_pref_name
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183,974 entries
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There is 0 pattern entry.
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FGLDS1
|
8115 |
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FS1
|
8115 |
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Mmt syndrome
|
8115 |
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Oded syndrome
|
8115 |
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oculodigitoesophagoduodenal syndrome
|
8115 |
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Feingold syndrome 1
|
8115 |
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MMT type 1
|
8115 |
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Feingold syndrome caused by mutation in MYCN
|
8115 |
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microcephaly-digital anomalies-normal intelligence syndrome type 1
|
8115 |
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pigmentary abnormality of the anterior segment of the eye
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C538115 |
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Epidermal hamartoma syndrome
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18115 |
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epidermal nevus syndrome
|
18115 |
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MYCN Feingold syndrome
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8115 |
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asymmetry in the pigmentation of the irides
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C538115 |
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Brunner-Winter syndrome type 1
|
8115 |
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