The search resulted in 53 diseases.
|
|
||
|---|---|---|---|
| Orphanet:137625 | Glycogen storage disease due to muscle and heart glycogen synthase deficiency | ||
| Orphanet:1479 | Atrial septal defect - atrioventricular conduction defects syndrome | ||
| Orphanet:1493 | Vici syndrome | ||
| Orphanet:217601 | Hypertrophic cardiomyopathy due to intensive athletic training | ||
| Orphanet:228012 | Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome | ||
| Orphanet:26791 | Multiple acyl-CoA dehydrogenase deficiency | ||
| Orphanet:308552 | Glycogen storage disease due to acid maltase deficiency, infantile onset | ||
| Orphanet:319678 | Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome | ||
| Orphanet:324 | Fabry disease | ||
| Orphanet:324525 | Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation | ||
| Orphanet:34587 | Glycogen storage disease due to LAMP-2 deficiency | ||
| Orphanet:366 | Glycogen storage disease due to glycogen debranching enzyme deficiency | ||
| Orphanet:500 | Noonan syndrome with multiple lentigines | ||
| Orphanet:54260 | Left ventricular noncompaction | ||
| Orphanet:550 | MELAS | ||
| Orphanet:551 | MERRF | ||
| Orphanet:59306 | McLeod neuroacanthocytosis syndrome | ||
| Orphanet:64 | Alström syndrome | ||
| Orphanet:93473 | Hurler syndrome | ||
| OMIM:115197 | Cardiomyopathy, familial hypertrophic, 4 | ||
| OMIM:192600 | Cardiomyopathy, familial hypertrophic, 1 | ||
| OMIM:229300 | Friedreich ataxia 1 | ||
| OMIM:601493 | Cardiomyopathy, dilated, 1C | ||
| OMIM:601494 | Cardiomyopathy, dilated, 1D | ||
| OMIM:604169 | Left ventricular noncompaction 1 | ||
| OMIM:607482 | Cardiomyopathy, dilated, 1M | ||
| OMIM:607487 | Cardiomyopathy, hypertrophic, 25 | ||
| OMIM:608751 | Cardiomyopathy, familial hypertrophic, 8 | ||
| OMIM:609909 | Cardiomyopathy, dilated, 1P | ||
| OMIM:612098 | Cardiomyopathy, familial hypertrophic, 11 | ||
| OMIM:612124 | Cardiomyopathy, familial hypertrophic, 12 | ||
| OMIM:612158 | Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction | ||
| OMIM:612422 | Cardiomyopathy, familial restrictive, 3 | ||
| OMIM:613172 | Cardiomyopathy, dilated, 1DD | ||
| OMIM:613251 | Cardiomyopathy, familial hypertrophic, 14 | ||
| OMIM:613424 | Cardiomyopathy, dilated, 1R | ||
| OMIM:613642 | Cardiomyopathy, dilated, 1GG | ||
| OMIM:613690 | Cardiomyopathy, familial hypertrophic, 7 | ||
| OMIM:613765 | Cardiomyopathy, familial hypertrophic, 9 | ||
| OMIM:613838 | Cardiomyopathy, familial hypertrophic, 16 | ||
| OMIM:613873 | Cardiomyopathy, familial hypertrophic, 17 | ||
| OMIM:613874 | Cardiomyopathy, familial hypertrophic, 18 | ||
| OMIM:613875 | Cardiomyopathy, familial hypertrophic, 19 | ||
| OMIM:613876 | Cardiomyopathy, familial hypertrophic, 20 | ||
| OMIM:613881 | Cardiomyopathy, dilated, 1HH | ||
| OMIM:614676 | Cardiomyopathy, familial hypertrophic, 21 | ||
| OMIM:615396 | Left ventricular noncompaction 10 | ||
| Orphanet:155 | Familial isolated hypertrophic cardiomyopathy | ||
| Orphanet:420429 | Glycogen storage disease due to acid maltase deficiency, late-onset | ||
| OMIM:615248 | Cardiomyopathy, dilated, 1KK | ||
| Orphanet:436242 | Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease | ||
| Orphanet:457185 | Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome | ||
| OMIM:617047 | CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26 |