HPO ID | HPO Term |
---|---|
HP:0001746 | Asplenia |
HP:0011599 | Mesocardia |
HP:0001651 | Dextrocardia |
HP:0003577 | Congenital onset |
HP:0000252 | Microcephaly |
HP:0002566 | Intestinal malrotation |
HP:0006695 | Atrioventricular canal defect |
HP:0001696 | Situs inversus totalis |
HP:0000006 | Autosomal dominant inheritance |
HP:0001748 | Polysplenia |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024