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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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type I Ehlers-Danlos syndrome
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19567 |
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injuries, blunt cardiac
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D000071956 |
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cardiac injuries, blunt
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D000071956 |
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cardiac injury, blunt
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D000071956 |
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calcinosis - Raynaud phenomenon - esophageal involvement - sclerodactyly - telangiectasia
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19563 |
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periodic systemic capillary leak syndrome
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1956 |
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limited cutaneous Systemic Scleroderma
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19563 |
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limited cutaneous Systemic sclerosis
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19563 |
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hereditary von Willebrand disease
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19565 |
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hereditary von Willebrand disease (hereditary or acquired)
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19565 |
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Cockayne syndrome caused by mutation in ERCC8
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19569 |
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injury, blunt cardiac
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D000071956 |
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Cockayne syndrome classic form
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19569 |
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Ehlers-Danlos syndrome, classic type, 1
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19567 |
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Ehlers-Danlos syndrome, classic type, 2
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19568 |
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