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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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leydig cell hypoplasia, complete
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C562567 |
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leydig cell hypoplasia, partial
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C562567 |
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leydig cell hypoplasia, type II
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C562567 |
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leydig cell hypoplasia, type i
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C562567 |
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hypergonadotropic hypogonadism, male, due to LHCGR defect
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C562567 |
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male hypergonadotropic hypogonadism due to LHCGR defect
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C562567 |
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type II leydig cell hypoplasia
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C562567 |
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type i leydig cell hypoplasia
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C562567 |
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lymphangiectasies and lymphedema Hennekam type
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16256 |
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intestinal lymphagiectasia lymphedema intellectual deficit syndrome
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16256 |
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Hennekam lymphangiectasia lymphedema syndrome
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16256 |
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male, due to LHCGR defect hypergonadotropic hypogonadism
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C562567 |
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gallbladder, agenesis of
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C562564 |
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infiltrating carcinoma of the breast
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6256 |
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invasive carcinoma of the breast
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6256 |
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