OMIM ID | Disease name | P-value |
---|---|---|
611126 | Deficiency of a Acyl-coa dehydrogenase family, member 9. | 1.5e-05 |
201450 | Deficiency of acyl-coa dehydrogenase, medium-chain. | 4.4e-05 |
201470 | Deficiency of acyl-coa dehydrogenase, short-chain. | 2.2e-05 |
201475 | Deficiency of acyl-coa dehydrogenase, very long-chain. | 4.2e-08 |
608810 | Alpha-b crystallinopathy. | 1.5e-05 |
205200 | Amyotrophic lateral sclerosis, juvenile, with dementia. | 5.1e-05 |
600996 | Arrhythmogenic right ventricular dysplasia, familial, 2; arvd2. | 7.9e-05 |
609160 | Arrhythmogenic right ventricular dysplasia, familial, 7. | 1.3e-05 |
604377 | Aardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase. | 4.7e-09 |
602067 | Cardiomyopathy, dilated, 1f; cmd1f. | 5.9e-05 |
192600 | Cardiomyopathy, familial hypertrophic 1; cmh1. | 7.4e-05 |
115210 | Cardiomyopathy, familial restrictive, 1; rcm1. | 7.1e-05 |
212350 | Cataract and cardiomyopathy. | 4.6e-07 |
601253 | Caveolin 3; cav3. | 7.8e-05 |
609060 | Combined oxidative phosphorylation deficiency 1; coxpd1. | 6.3e-05 |
610505 | Combined oxidative phosphorylation deficiency 3; coxpd3. | 4.4e-08 |
611719 | Combined oxidative phosphorylation deficiency 5; coxpd5. | 9.9e-07 |
300257 | Danon disease. | 6.1e-06 |
602668 | Dystrophia myotonica 2; dm2. | 3.6e-05 |
158900 | Facioscapulohumeral muscular dystrophy 1a; fshmd1a. | 2.4e-05 |
229300 | Friedreich ataxia 1; frda. | 5.5e-05 |
253800 | Fukuyama congenital muscular dystrophy; fcmd. | 8.8e-05 |
232300 | Glycogen storage disease ii. | 4.9e-06 |
232400 | Glycogen storage disease iii. | 5.3e-06 |
261740 | Glycogen storage disease of heart, lethal congenital. | 5.7e-06 |
261670 | Glycogen storage disease x; gsd10. | 4.4e-06 |
600737 | Inclusion body myopathy 2, autosomal recessive; ibm2. | 8.8e-05 |
167320 | Inclusion body myopathy with early-onset paget disease and frontotemporal. | 5.3e-05 |
147421 | Inclusion body miositis. | 2.4e-05 |
606183 | Laryngeal abductor paralysis with cerebellar ataxia and motor neuropathy. | 1.9e-05 |
220111 | Leigh syndrome, French-Canadian type; lsfc. | 7.8e-05 |
300322 | Lesch-nyhan syndrome; lns. | 8.9e-05 |
109150 | Machado-joseph disease; mjd. | 8.1e-05 |
248800 | Marinesco-sjogren syndrome; mss. | 7.9e-05 |
252011 | Mitochondrial complex ii deficiency. | 6.7e-06 |
609560 | Mitochondrial DNA depletion syndrome, myopathic form. | 3.4e-08 |
600462 | Mitochondrial myopathy and sideroblastic anemia; mlasa. | 7.2e-05 |
500002 | Mitochondrial myopathy with diabetes. | 3.1e-06 |
251950 | Mitochondrial myopathy with lactic acidosis. | 2.5e-05 |
610773 | Mitochondrial phosphate carrier deficiency. | 5.5e-08 |
310200 | Muscular dystrophy, duchenne type; dmd. | 9.5e-05 |
605809 | Myasthenia, familial infantile, 1. | 2.3e-07 |
610542 | Myasthenia, limb-girdle, with tubular aggregates. | 4.9e-06 |
254210 | Myasthenic syndrome, congenital, associated with episodic apnea. | 5.2e-07 |
255125 | Myopathy with lactic acidosis, hereditary; hml | 3.9e-07 |
609500 | Myopathy, autophagic vacuolar, infantile-onset. | 3.6e-05 |
609200 | Myotilinopathy. | 2.6e-05 |
258450 | Progressive external ophthalmoplegia with mitochondrial dna deletions. | 1.2e-05 |
609286 | Progressive external ophthalmoplegia with mitochondrial dna deletions. | 2.1e-06 |
212138 | Solute carrier family 25 (carnitine/acylcarnitine translocase), member. | 4.3e-06 |
103220 | Solute carrier family 25 (mitochondrial carrier, adenine nucleotide. | 3.9e-06 |
604360 | Spastic paraplegia 11, autosomal recessive; spg11. | 9.4e-05 |
610250 | Spastic paraplegia 31, autosomal dominant; spg31. | 8.4e-05 |
183020 | Spinal muscular atrophy, segmental. | 7.7e-05 |
253300 | Spinal muscular atrophy, type i; sma1. | 6.2e-05 |
609015 | Trifunctional protein deficiency. | 2.9e-06 |
222300 | Wolfram syndrome 1; wfs1. | 7.5e-05 |