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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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deficiencies, 7-dehydrocholesterol reductase
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D019082 |
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deficiency, 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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extensively drug resistant tuberculosis
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D054908 |
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extremely drug resistant tuberculosis
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D054908 |
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CTNNA3 arrhythmogenic right ventricular cardiomyopathy
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908 |
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familial arrhythmogenic right ventricular dysplasia 13
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908 |
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chromosome 15 ring
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19908 |
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BCG and salmonella infection, disseminated
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C565908 |
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congenital profound sensorineural deafness and oligodontia
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9089 |
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autosomal recessive sensorineural hearing impairment, dizziness, and hypodontia
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9089 |
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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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