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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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autoimmune hypothyroidism
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C562768 |
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childhood onset IBGC
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C536276 |
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idiopathic, childhood-onset basal ganglia calcification
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C536276 |
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childhood onset bilateral striopallidodentate calcinosis
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C536276 |
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bilateral striopallidodentate calcinosis, childhood onset
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C536276 |
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congenital, 1 capillary malformations
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C562760 |
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high-grade neuroendocrine carcinoma of the cervix uteri
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16276 |
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high-grade neuroendocrine carcinoma of the uterine cervix
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16276 |
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nonarteriosclerotic, idiopathic, childhood-onset cerebral calcification
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C536276 |
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capillary malformations, congenital, 1
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C562760 |
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idiopathic basal ganglia calcification, childhood onset
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C536276 |
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childhood onset idiopathic basal ganglia calcification
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C536276 |
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genetic defect in, 3 thyroid hormonogenesis
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C562769 |
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inflammatory myofibroblastic lung tumor
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6276 |
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lung inflammatory myofibroblastic tumor
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6276 |
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