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:0004749 | HP:0004749 | Atrial flutter | 0 | ACTC1 CL E G H | 70 | 143 | ORPHA:99103 | Atrial septal defect, ostium secundum type | HP:0040283 - Occasional | | | 208 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | ACTC1 CL E G H | 70 | 143 | OMIM:612098 | Cardiomyopathy, familial hypertrophic, 11 | | | | 208 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | CITED2 CL E G H | 10370 | 1987 | ORPHA:99103 | Atrial septal defect, ostium secundum type | HP:0040283 - Occasional | | | 5 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | CITED2 CL E G H | 10370 | 1987 | ORPHA:99105 | Atrial septal defect, sinus venosus type | HP:0040283 - Occasional | | | 5 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | CLIC2 CL E G H | 1193 | 2063 | ORPHA:324410 | X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome | HP:0040283 - Occasional | | | 4 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | CYTB CL E G H | 4519 | 7427 | ORPHA:137675 | Histiocytoid cardiomyopathy | HP:0040284 - Very rare | | | | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | DMPK CL E G H | 1760 | 2933 | OMIM:160900 | Myotonic dystrophy 1 | | | | 152 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | GATA4 CL E G H | 2626 | 4173 | ORPHA:99103 | Atrial septal defect, ostium secundum type | HP:0040283 - Occasional | | | 87 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | GATA6 CL E G H | 2627 | 4174 | ORPHA:99103 | Atrial septal defect, ostium secundum type | HP:0040283 - Occasional | | | 37 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | KCNK3 CL E G H | 3777 | 6278 | OMIM:615344 | Pulmonary hypertension, primary, 4 | | | | 7 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | LMNA CL E G H | 4000 | 6636 | OMIM:115200 | Cardiomyopathy, dilated, 1A | . | | | 645 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | LMNA CL E G H | 4000 | 6636 | ORPHA:300751 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | HP:0040283 - Occasional | | | 645 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | MYH6 CL E G H | 4624 | 7576 | ORPHA:99103 | Atrial septal defect, ostium secundum type | HP:0040283 - Occasional | | | 452 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | NKX2-5 CL E G H | 1482 | 2488 | ORPHA:99103 | Atrial septal defect, ostium secundum type | HP:0040283 - Occasional | | | 90 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | NUP155 CL E G H | 9631 | 8063 | OMIM:615770 | Atrial fibrillation, familial, 15 | . | | | 1 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | PRKAG2 CL E G H | 51422 | 9386 | OMIM:194200 | WOLFF-PARKINSON-WHITE SYNDROME | | | | 235 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | SCN3B CL E G H | 55800 | 20665 | OMIM:613120 | Brugada syndrome 7 | . | | | 122 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | SCN5A CL E G H | 6331 | 10593 | OMIM:614022 | Atrial fibrillation, familial, 10 | HP:0040283 - Occasional | | | 1134 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | SCN5A CL E G H | 6331 | 10593 | OMIM:601144 | BRUGADA SYNDROME 1; BRGDA1 | | | | 1134 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | SCN5A CL E G H | 6331 | 10593 | OMIM:601154 | Cardiomyopathy, dilated, 1E | . | | | 1134 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | SGO1 CL E G H | 151648 | 25088 | OMIM:616201 | Chronic atrial and intestinal dysrhythmia | HP:0040283 - Occasional | | | 2 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | TBX20 CL E G H | 57057 | 11598 | ORPHA:99103 | Atrial septal defect, ostium secundum type | HP:0040283 - Occasional | | | 20 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | TLL1 CL E G H | 7092 | 11843 | ORPHA:99106 | Atrial septal defect, ostium primum type | HP:0040283 - Occasional | | | 6 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | TLL1 CL E G H | 7092 | 11843 | ORPHA:99103 | Atrial septal defect, ostium secundum type | HP:0040283 - Occasional | | | 6 | | |
HP:0004749 | HP:0004749 | Atrial flutter | 0 | TNNI3K CL E G H | 51086 | 19661 | OMIM:616117 | Cardiac conduction disease with or without dilated cardiomyopathy | . | | | 1 | | |
HP:0004749 | HP:0031672 | Reverse typical atrial flutter | 1 | CL E G H | | | | | | | | | | |
HP:0004749 | HP:0031671 | Typical atrial flutter | 1 | CL E G H | | | | | | | | | | |