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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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angiopathy, cerebral amyloid
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D016657 |
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sporadic cerebral amyloid angiopathy
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D016657 |
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familial, autosomal dominant periodic fever
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C536657 |
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periodic fever, familial, autosomal dominant
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C536657 |
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familial hibernian fever
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C536657 |
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hibernian familial fever
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C536657 |
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spondyloepimetaphyseal dysplasia, missouri type
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C566574 |
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apparent mineralocorticoid excess syndrome
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6657 |
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hibernian fever, familial
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C536657 |
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TNF Receptor-associated periodic syndrome (TRAPS)
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C536657 |
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missouri type spondyloepimetaphyseal dysplasia
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C566574 |
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SEMD, missouri type
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C566574 |
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8p11.2 deletion syndrome
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16657 |
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usher syndrome, type IE
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C566577 |
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focal adult-onset torsion dystonia
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C566572 |
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