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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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spastic ataxia, autosomal recessive
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17847 |
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skin of body hypersensitivity reaction type II disease
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17841 |
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Moyamoya disease caused by mutation in RNF213
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11784 |
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RNF213 Moyamoya disease
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11784 |
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malignant renal hypertension
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1784 |
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malignant renovascular hypertension
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1784 |
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cutaneous T-cell lymphoma/Sezary syndrome
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17844 |
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partial deletion of chromosome 12p
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17848 |
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partial monosomy of chromosome 12p
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17848 |
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congenital sequestration of lung
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17843 |
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autoimmune disease of skin and connective tissue
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17841 |
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partial deletion of the short arm of chromosome 12
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17848 |
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partial monosomy of the short arm of chromosome 12
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17848 |
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partial deletion of the short arm of chromosome type 12
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17848 |
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integument hypersensitivity reaction type II disease
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17841 |
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