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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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APS type 2
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10012 |
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delta1-pyrroline-5-carboxylate synthetase deficiency
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100126 |
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X-linked syndromic intellectual disability caused by mutation in NAA10
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100124 |
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vector-borne infectious disease
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100120 |
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hallucinogen-persisting perception disorder
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100125 |
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autoimmune thyroid disease and/or type 1 diabetes-Addison disease syndrome
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10012 |
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arachnoid cysts, intracranial
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100129 |
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NAA10 X-linked syndromic intellectual disability
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100124 |
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myopathy with ptosis and mild dystrophic pattern
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100121 |
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autoimmune polyendocrine syndrome type 2
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10012 |
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autoimmune polyglandular syndrome type 2
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10012 |
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polyglandular deficiency syndrome type 2
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10012 |
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congenital myopathy with severe fetal hypokinesia
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100121 |
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polyendocrine autoimmune syndrome, type 2
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10012 |
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polyglandular autoimmune syndrome, type 2
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10012 |
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