| Diseases |
Alias |
|
| Hypomagnesemia, Hypertension, And Hypercholesterolemia, Mitochondrial |
|
|
| Myoclonic Epilepsy Associated With Ragged-Red Fibers |
-
Merrf Syndrome
-
MERRF
-
Fukuhara Syndrome
-
Myoclonic Epilepsy Associated With Ragged Red Fibers
-
Myoencephalopathy Ragged-Red Fiber Disease
-
Myoclonic Epilepsy - Ragged Red Fibers
-
Myoclonus Epilepsy And Ragged Red Fibers
-
Myoclonus With Epilepsy And With Ragged Red Fibers
-
Myoclonic Epilepsy With Ragged Red Fibers
-
Myoclonic Epilepsy With Ragged-Red Fibers
-
Fukuhara Disease
-
Myoclonus Epilepsy Associated With Ragged-Red Fibres
-
Myoclonus With Epilepsy With Ragged Red Fibers
|
|
| Cardiomyopathy, Familial Hypertrophic, 1 |
-
Asymmetric Septal Hypertrophy
-
Familial Hypertrophic Cardiomyopathy
-
Hypertrophic Cardiomyopathy 1
-
CMH1
-
Hypertrophic Cardiomyopathy 19
-
CMH
-
Ventricular Hypertrophy, Hereditary
-
Ash
-
Hypertrophic Subaortic Stenosis, Idiopathic
-
Cardiomyopathy, Familial Hypertrophic
-
Cardiomyopathy, Hypertrophic, 1, Digenic
-
Cardiomyopathy, Familial Hypertrophic 1
-
Hcm
-
Hereditary Ventricular Hypertrophy
-
Idiopathic Hypertrophic Subaortic Stenosis
-
Hypertrophic Cardiomyopathy
-
Cardiomyopathy, Hypertrophic, Familial
-
Cardiomyopathy, Hypertrophic, 1
-
Familial Asymmetric Septal Hypertrophy
-
Heritable Hypertrophic Cardiomyopathy
-
Fhc
-
Cardiomyopathy, Hypertrophic, Familial, Type 1
|
|
| Deafness, Nonsyndromic Sensorineural, Mitochondrial |
-
Mitochondrial Non-Syndromic Sensorineural Hearing Loss
-
Mitochondrial Nonsyndromic Sensorineural Deafness
-
Mitochondrial Non-Syndromic Sensorineural Deafness
-
Isolated Mitochondrial Neurosensory Deafness
-
Isolated Mitochondrial Neurosensory Hearing Loss
-
Isolated Mitochondrial Sensorineural Deafness
-
Isolated Mitochondrial Sensorineural Hearing Loss
-
Mitochondrial Non-Syndromic Neurosensory Deafness
-
Mitochondrial Non-Syndromic Neurosensory Hearing Loss
-
Deafness, Sensorineural, Mitochondrial
-
DFNM
|
|
| Mitochondrial Disease |
-
Mitochondrial Diseases
-
Mitochondrial Disorder
|
|
| Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes |
-
Melas Syndrome
-
MELAS
-
Mitochondrial Encephalomyopathy Lactic Acidosis And Stroke-Like Episodes
-
Mitochondrial Myopathy, Lactic Acidosis, Stroke-Like Episode
-
Mitochondrial Encephalomyopathy, Lactic Acidosis, And Stroke-Like Episodes
-
Myopathy, Mitochondrial-Encephalopathy-Lactic Acidosis-Stroke
-
Mitochondrial Encephalomyopathy, Lactic Acidosis And Stroke-Like Episodes
-
Mitochondrial Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes
-
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis And Stroke-Like Episodes
-
Mitochondrial Encephalomyopathy With Lactic Acidosis And Stroke-Like Episodes Syndrome
-
Myopathy, Mitochondrial, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes
|
|
| Dilated Cardiomyopathy |
-
Familial Dilated Cardiomyopathy
-
Primary Dilated Cardiomyopathy
-
Idiopathic Dilated Cardiomyopathy
-
Congestive Cardiomyopathy
-
Idiopathic Dilation Cardiomyopathy
-
Primary Familial Dilated Cardiomyopathy
-
Cardiomyopathy, Dilated
-
DCM
-
Cardiomyopathy, Familial Dilated
-
Dilated Cardiomyopathy, Familial
-
Hypokinetic Dilated Cardiomyopathy, Familial
-
Familial Idiopathic Cardiomyopathy
-
Fdc
-
Cardiomyopathy, Familial Idiopathic
-
Idiopathic Cardiomegaly
-
Dilated Congestive Cardiomyopathy
-
Chronic Dilated Cardiomyopathy
-
Ccm - [Congestive Cardiomyopathy]
-
Cocm - [Congestive Cardiomyopathy]
-
Dcm - [Dilated Cardiomyopathy]
-
Dilated-Hypokinetic Cardiomyopathy
-
Congestive Idiopathic Cardiomyopathy
-
Primary Idiopathic Dilated Cardiomyopathy
|
|
| Kenny-Caffey Syndrome, Type 1 |
-
KCS1
-
Kenny-Caffey Syndrome Type 1
-
Autosomal Recessive Kenny-Caffey Syndrome
-
Kcs
-
Kenny-Caffey Syndrome, Autosomal Recessive
-
Kenny-Caffey Syndrome 1
-
Kenny-Caffey Syndrome Autosomal Recessive
-
Kenny-Caffey Syndrome-1
|
|
| Kearns-Sayre Syndrome |
-
Ophthalmoplegia
-
Mitochondrial Cytopathy
-
KSS
-
Ophthalmoplegia, Pigmentary Degeneration Of Retina, And Cardiomyopathy
-
Oculocraniosomatic Syndrome
-
Chronic Progressive External Ophthalmoplegia With Myopathy
-
Cpeo With Myopathy
-
Total Ophthalmoplegia
-
Ophthalmoplegia-Plus Syndrome
-
Ophthalmoplegia, Progressive External, With Ragged-Red Fibers
-
Cpeo With Ragged-Red Fibers
-
Oculomotor Paralysis
-
Renal Tubulopathy, Diabetes Mellitus, And Cerebellar Ataxia Due To Duplication O
-
Renal Tubulopathy, Diabetes Mellitus, And Cerebellar Ataxia Due To Duplication Of Mitochondrial Dna
-
Proximal Tubulopathy, Diabetes Mellitus And Cerebellar Ataxia
-
Cpeo With Ragged Red Fibers
-
Ophthalmoplegia Plus Syndrome
-
Ophthalmoplegia, Progressive External, With Ragged Red Fibers
-
Kearns-Sayre Mitochondrial Cytopathy
-
Mitochondrial Myopathies
|
|
| Leber Hereditary Optic Neuropathy, Modifier Of |
-
Leber Optic Atrophy
-
Leber Hereditary Optic Neuropathy
-
LHON
-
Leber'S Hereditary Optic Neuropathy
-
Leber Optic Atrophy, Susceptibility To
-
Leber'S Optic Atrophy
-
LOAM
-
Loas
-
Leber'S Disease
-
Leber'S Optic Neuropathy
-
Optic Atrophy, Hereditary, Leber
-
Lhon, Modifier Of
-
Optic Atrophy, Leber Type
-
Hereditary Optic Neuroretinopathy
-
Leber Hereditary Optic Atrophy
-
Loa
-
Optic Atrophy Leber Type
-
Leber Hereditary Optic Neuropathy, Modifier
-
Leber Hereditary Optic Neuropathy Susceptibility
-
Modifier Of Leber Hereditary Optic Neuropathy
-
Lebers Hereditary Optic Neuropathy
-
Leber Congenital Amaurosis
|
|