Mitochondrial Myopathy with a Defect in Mitochondrial Protein Transport - Ontology Browser

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Mitochondrial Myopathy with a Defect in Mitochondrial Protein Transport (DOID:9004925)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)

Parent Terms

Term With Siblings

Child Terms

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, Lethal Infantile

Mitochondrial Progressive Myopathy with Congenital Cataract, Hearing Loss, and Developmental Delay

MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT

myopathy, lactic acidosis, and sideroblastic anemia +

NARP syndrome

Synonyms
Primary IDs:	MESH:C565376 ; RDO:0014027

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