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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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T-lymphocyte deficiency (finding)
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3780 |
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teratoma, benign (morphologic abnormality)
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2378 |
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8p- syndrome (partial)
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C537826 |
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partial deletion (short arm) chromosome 8
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C537826 |
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deletion 8p23 1
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C537827 |
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monosomy 8p23 1
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C537827 |
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rhabdomyosarcoma embryonal 1
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C537883 |
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lattice type 1 CDL1 corneal dystrophy
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C537881 |
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distal, type 1 arthrogryposis
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C535378 |
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distal type 1 arthrogryposis multiplex congenita
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C535378 |
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monosomy 8p23 1 chromosome 8
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C537827 |
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lattice type 1 corneal dystrophy
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C537881 |
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corneal type 1 macular dystrophy
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C537834 |
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congenital motor, 1 nystagmus
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C537853 |
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partial trisomy 10q
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C537804 |
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