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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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netherton disease
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D056770 |
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netherton syndrome
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D056770 |
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autosomal recessive 13 mental retardation
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C567714 |
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cardiac diverticulum (disease)
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15677 |
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benign neonatal, 1, atypical severe epilepsy
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C567745 |
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brugada syndrome 7
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C567734 |
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central areolar 2 choroidal dystrophy
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C567750 |
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3-Hydroxy-3-Methylglutaryl-CoA synthase 2 deficiency
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C567784 |
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familial juvenile 2 hyperuricemic nephropathy
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C567760 |
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benign recurrent, 2 vertigo
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C567749 |
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dermatitis, atopic, 7
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C567796 |
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brugada syndrome 8
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C567732 |
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hereditary transthyretin amyloidosis
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C567782 |
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central areolar 3 choroidal dystrophy
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C567729 |
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complete, cbx2-related 46,xy gonadal dysgenesis
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C567766 |
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