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:0011711 | HP:0011711 | Left anterior fascicular block | 0 | ACTC1 CL E G H | 70 | 143 | OMIM:612098 | Cardiomyopathy, familial hypertrophic, 11 | | | | 208 | | |
HP:0011711 | HP:0011711 | Left anterior fascicular block | 0 | FLNC CL E G H | 2318 | 3756 | OMIM:617047 | Cardiomyopathy, familial hypertrophic, 26 | | | | 197 | | |
HP:0011711 | HP:0011711 | Left anterior fascicular block | 0 | LMNA CL E G H | 4000 | 6636 | OMIM:181350 | Emery-Dreifuss muscular dystrophy 2, autosomal dominant | | | | 645 | | |
HP:0011711 | HP:0011711 | Left anterior fascicular block | 0 | MYH7 CL E G H | 4625 | 7577 | ORPHA:437572 | MYH7-related late-onset scapuloperoneal muscular dystrophy | HP:0040283 - Occasional | | | 1269 | | |
HP:0011711 | HP:0011711 | Left anterior fascicular block | 0 | SCN5A CL E G H | 6331 | 10593 | OMIM:113900 | Progressive familial heart block, type IA | . | | | 1134 | | |
HP:0011711 | HP:0011711 | Left anterior fascicular block | 0 | TNNC1 CL E G H | 7134 | 11943 | OMIM:613243 | Cardiomyopathy, familial hypertrophic, 13 | HP:0040283 - Occasional | | | 73 | | |
HP:0011711 | HP:0011711 | Left anterior fascicular block | 0 | TNNI3K CL E G H | 51086 | 19661 | OMIM:616117 | Cardiac conduction disease with or without dilated cardiomyopathy | | | | 1 | | |
HP:0011711 | HP:0011711 | Left anterior fascicular block | 0 | TRPM4 CL E G H | 54795 | 17993 | OMIM:604559 | Progressive familial heart block, type IB | . | | | 124 | | |