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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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bangstad syndrome
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C537902 |
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lichen planus, familial
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7902 |
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autosomal recessive MSMD due to partial IFNgammaR2 deficiency
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17902 |
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autosomal recessive MSMD due to partial interferon gamma receptor 2 deficiency
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17902 |
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autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in IFNGR2
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17902 |
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autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
|
17902 |
|
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autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 2 deficiency
|
17902 |
|
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hereditary lichen planus
|
7902 |
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IFNGR2 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency
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17902 |
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