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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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complementation group e peroxisome biogenesis disorder
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C566569 |
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adenocarcinoma of extrahepatic bile duct
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2665 |
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alzheimer disease, familial, 5
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C566578 |
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periodic fever, familial, autosomal dominant
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C536657 |
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familial, 2 febrile convulsions
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C566541 |
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apparent mineralocorticoid excess syndrome
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6657 |
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seizures, familial febrile, 2
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C566541 |
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familial hibernian fever
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C536657 |
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palsy of facial nerve
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5665 |
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hibernian familial fever
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C536657 |
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congenital, 2 fibrosis of extraocular muscles
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C566587 |
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cleft palate, hearing loss, and camptodactyly facial dysmorphism
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C566524 |
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hibernian fever, familial
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C536657 |
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chronic atrophic gastritis
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6665 |
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familial infantile gigantism due to a point mutation
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18665 |
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