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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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chromosome 5q14.3 deletion syndrome
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16456 |
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primary thymic epithelial neoplasm
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6456 |
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primary thymic epithelial tumor
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6456 |
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progressive, and hypogonadotropic hypogonadism adrenal insufficiency
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C564568 |
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x-linked 58 mental retardation
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C564566 |
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congenital, with precocious puberty adrenal hypoplasia
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C564568 |
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autosomal dominant intellectual disability 20
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16456 |
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x-linked, 2 lissencephaly
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C564563 |
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x-linked episodic muscle weakness
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C564565 |
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5q14.3 deletion syndrome
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16456 |
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5q14.3 microdeletion syndrome
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16456 |
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17beta-Hydroxysteroid dehydrogenase type 10 deficiency
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C564560 |
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simpson-golabi-behmel syndrome, type 2
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C564567 |
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3-Hydroxyacyl-CoA dehydrogenase, type 2, deficiency
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C564560 |
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Hydroxyacyl-CoA dehydrogenase, type 2, deficiency
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C564560 |
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