Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: |
HPO disease - gene - phenotype less frequent non-typical associations: |
HP:0032296 | HP:0032296 | Increased circulating IgG subclass | 0 | IFIH1 CL E G H | 64135 | 18873 | OMIM:619773 | IMMUNODEFICIENCY 95; IMD95 | | | | 28 | | |
HP:0032296 | HP:0032298 | Increased circulating IgG1 level | 1 | CL E G H | | | | | | | | | | |
HP:0032296 | HP:0032300 | Increased circulating IgG4 level | 1 | CL E G H | | | | | | | | | | |
HP:0032296 | HP:0032299 | Increased circulating IgG2 level | 1 | CL E G H | | | | | | | | | | |
HP:0032296 | HP:0032297 | Increased circulating IgG3 level | 1 | IFIH1 CL E G H | 64135 | 18873 | OMIM:619773 | IMMUNODEFICIENCY 95; IMD95 | | | | 28 | | |