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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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fasps
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C565789 |
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mediastinal lipomatosis
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6578 |
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adolescent nephronophthisis
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C565780 |
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nephronophthisis, adolescent
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C565780 |
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fatal infantile, due to cytochrome c oxidase deficiency cardioencephalomyopathy
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C565784 |
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familial febrile, 4 convulsions
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C565788 |
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familial febrile, 4 seizures
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C565788 |
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alzheimer disease 5
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C566578 |
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familial, with cleft palate and cerebellar hypoplasia lissencephaly
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C565781 |
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familial, 5 alzheimer disease
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C566578 |
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OXPHOS disease due to nDNA anomalies
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16578 |
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OXPHOS disease due to nuclear DNA anomalies
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16578 |
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congenital deafness, macular dystrophy, and psychiatric disorders myoclonic epilepsy
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C565786 |
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febrile convulsions, familial, 4
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C565788 |
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alzheimer disease, familial, 5
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C566578 |
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