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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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ebv-associated, autosomal, 1 lymphoproliferative syndrome
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C567815 |
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paroxysmal familial, 1 ventricular fibrillation
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C567851 |
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parkinson disease 14, autosomal recessive
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C567844 |
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spastic quadriplegic, 2 cerebral palsy
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C567867 |
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paroxysmal familial, 2 ventricular fibrillation
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C567841 |
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familial febrile, 3a convulsions
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C567820 |
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familial febrile, 3a seizures
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C567820 |
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optic atrophy 7
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C567833 |
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VWM syndrome, CACH
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D056784 |
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syndrome, CACH VWM
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D056784 |
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group c XP
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C567886 |
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oligodactylous clubfeet, and anonychia-nail hypoplasia syndrome fibular agenesis-hypoplasia
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C567819 |
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vascular malformations, and epidermal nevi congenital lipomatous overgrowth
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C567863 |
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unusual facies, and large feet occipital atretic cephalocele
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C567865 |
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marfanoid habitus and specific language and learning disabilities
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C567864 |
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