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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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acrodysgenital syndrome, lethal
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D019082 |
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acrodysgenital syndromes, lethal
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D019082 |
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deficiencies, 7-dehydrocholesterol reductase
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D019082 |
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sex reversal, renal hypoplasia, and unilobar lung polydactyly
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D019082 |
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smith lemli opitz syndrome
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D019082 |
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smith lemli opitz syndrome, type 1
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D019082 |
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smith lemli opitz syndrome, type 2
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D019082 |
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smith lemli opitz syndrome, type II
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D019082 |
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smith lemli opitz syndrome, type i
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D019082 |
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rutledge lethal multiple congenital anomaly syndrome
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D019082 |
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deficiency, 7-dehydrocholesterol reductase
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D019082 |
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type 1 smith lemli opitz syndrome
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D019082 |
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type 2 smith lemli opitz syndrome
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D019082 |
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type II smith lemli opitz syndrome
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D019082 |
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type i smith lemli opitz syndrome
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D019082 |
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