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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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MMDS2
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13675 |
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BOLA3 deficiency
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13675 |
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deletion xq28
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C536755 |
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monosomy xq28
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C536755 |
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duplication xp3
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C536756 |
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trisomy xp3
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C536756 |
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gustavson syndrome
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C536759 |
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multiple mitochondrial dysfunctions syndrome 2
|
13675 |
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nonsyndromic, 9 cleft lip with or without cleft palate
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C563675 |
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duplication xq13 1 q21 1
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C536753 |
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trisomy xq13 1 q21 1
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C536753 |
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duplication xq13 1 q21 1 x chromosome
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C536753 |
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mental retardation X-linked severe gustavson type
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C536759 |
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facial nevi and mental changes arteriovenous aneurysm of mid-brain and retina
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C536752 |
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multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia
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13675 |
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