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:0011907 | HP:0011907 | Reduced alpha/beta synthesis ratio | 0 | ATRX CL E G H | 546 | 886 | OMIM:300448 | ALPHA-THALASSEMIA MYELODYSPLASIA SYNDROME; ATMDS | | | | 169 | | |
HP:0011907 | HP:0011907 | Reduced alpha/beta synthesis ratio | 0 | ATRX CL E G H | 546 | 886 | OMIM:301040 | Alpha-Thalassemia/mental retardation syndrome, X-linked | . | | | 169 | | |
HP:0011907 | HP:0011907 | Reduced alpha/beta synthesis ratio | 0 | HBA1 CL E G H | 3039 | 4823 | OMIM:604131 | ALPHA-THALASSEMIA | . | | | 200 | | |
HP:0011907 | HP:0011907 | Reduced alpha/beta synthesis ratio | 0 | HBA1 CL E G H | 3039 | 4823 | OMIM:613978 | Hemoglobin H disease | . | | | 200 | | |
HP:0011907 | HP:0011907 | Reduced alpha/beta synthesis ratio | 0 | HBA2 CL E G H | 3040 | 4824 | OMIM:604131 | ALPHA-THALASSEMIA | . | | | 88 | | |
HP:0011907 | HP:0011907 | Reduced alpha/beta synthesis ratio | 0 | HBA2 CL E G H | 3040 | 4824 | OMIM:613978 | Hemoglobin H disease | . | | | 88 | | |
HP:0011907 | HP:0011907 | Reduced alpha/beta synthesis ratio | 0 | HBB CL E G H | 3043 | 4827 | OMIM:604131 | ALPHA-THALASSEMIA | . | | | 580 | | |
HP:0011907 | HP:0011907 | Reduced alpha/beta synthesis ratio | 0 | HBB CL E G H | 3043 | 4827 | ORPHA:90039 | Hemoglobin D disease | | | | 580 | | |