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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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von willebrand disease, type i
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D056725 |
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deafness, autosomal dominant, due to mutation in Myo1a
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C567266 |
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autosomal dominant, due to mutation in Myo1a deafness
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C567266 |
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epidermolysis bullosa dystrophica with subcorneal cleavage
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C567272 |
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deafness, autosomal dominant 2b
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C567214 |
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deafness, autosomal dominant 3a
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C567277 |
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deafness, autosomal dominant 3b
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C567215 |
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type 6 episodic ataxia
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C567207 |
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1q21.1 contiguous gene deletion
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C567291 |
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febrile convulsions, familial, 10
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C567218 |
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familial, 10 febrile convulsions
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C567218 |
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seizures, familial febrile, 10
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C567218 |
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autosomal dominant hypercarotenemia and vitamin a deficiency
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C567296 |
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autosomal recessive inflammatory bowel disease 25
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C567251 |
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amelogenesis imperfecta, hypomaturation type, iia2
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C567279 |
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