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Term:
mitochondrial myopathy
(DOID:699)
Annotations:
Rat: (111)
Mouse: (134)
Human: (143)
Chinchilla: (98)
Bonobo: (98)
Dog: (110)
Squirrel: (98)
Pig: (109)
Parent Terms
Term With Siblings
Child Terms
Mitochondrial Cytopathy
+
myopathy
+
Alcohol Myopathy
centronuclear myopathy
+
congenital myopathy
+
congenital structural myopathy
+
Kearns-Sayre syndrome
King Denborough syndrome
mitochondrial myopathy
+
A myopathy that is characterized by mitochondrial dysfunction. (DO)
Multiple Epiphyseal Dysplasia with Myopathy
muscular atrophy
+
muscular dystrophy
+
Myoectodermal Gonadal Dysgenesis Syndrome
myofascial pain syndrome
+
myofibrillar myopathy
+
myoglobinuria
+
Myopathy due to Malate-Aspartate Shuttle Defect
MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY
myopathy of extraocular muscle
+
myopathy with extrapyramidal signs
Myopathy with Giant Abnormal Mitochondria
Myopathy with Myalgia, increased Serum Creatine Kinase, and with or without Episodic Rhabdomyolysis
Myopathy, Cataract, Hypogonadism Syndrome
Myopathy, Epilepsy, and Progressive Cerebral Atrophy
myositis
+
Myostitis
neurogenic scapuloperoneal syndrome Kaeser type
Neutral Lipid Storage Disease with Myopathy
Oculopharyngeal Myopathy with Leukoencephalopathy 1
polymyalgia rheumatica
Reducing Body Myopathies
+
rhabdomyolysis-myalgia syndrome
Secretory Diarrhea, Myopathy, and Deafness
Tubular Aggregate Myopathies
+
X-linked myopathy with excessive autophagy
chronic progressive external ophthalmoplegia
+
combined oxidative phosphorylation deficiency 3
Episodic Mitochondrial Myopathy with or without Optic Atrophy and Reversible Leukoencephalopathy
mitochondrial DNA depletion syndrome 11
mitochondrial DNA depletion syndrome 12a
mitochondrial DNA depletion syndrome 12b
mitochondrial DNA depletion syndrome 14
mitochondrial DNA depletion syndrome 15
Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form, Autosomal Recessive
+
mitochondrial encephalomyopathy
+
Mitochondrial Myopathy with a Defect in Mitochondrial Protein Transport
Mitochondrial Myopathy with Diabetes
Mitochondrial Myopathy with Lactic Acidosis
Mitochondrial Myopathy, and Ataxia
Mitochondrial Myopathy, Infantile, Transient
MITOCHONDRIAL MYOPATHY, ISOLATED, AUTOSOMAL DOMINANT
Mitochondrial Myopathy, Lethal Infantile
Mitochondrial Progressive Myopathy with Congenital Cataract, Hearing Loss, and Developmental Delay
myopathy, lactic acidosis, and sideroblastic anemia
+
NARP syndrome
Synonyms
Exact Synonyms:
Luft disease ; Luft's Disease ; Lufts Disease ; Megaconial Myopathy ; Mitochondrial Myopathies ; Pleoconial Myopathies ; megaconial myopathies ; pleoconial myopathy
Narrow Synonyms:
MITOCHONDRIAL MYOPATHY, ISOLATED ; MYOPATHY, MITOCHONDRIAL, LATE-ONSET ; MYOTONIC DYSTROPHY-LIKE MYOPATHY ; skeletal myopathy, responsive to riboflavin
Primary IDs:
MESH:D017240
Alternate IDs:
OMIM:251900
Xrefs:
NCI:C101328
Definition Sources:
http://en.wikipedia.org/wiki/Mitochondrial_myopathies
"DO" "DO",
http://www.ninds.nih.gov/disorders/mitochondrial_myopathy/mitochondrial_myopathy.htm
"DO" "DO"