Mondo Disease Ontology
3949 terms(s) returned
| Term Type: | Record: 2751 to 2800 of 3949 Records | Page: 56 of 79, First Previous Next Last | Show Records Per Page |
- mitochondrial complex IV deficiency, nuclear type 3
- mitochondrial complex IV deficiency, nuclear type 4
- mitochondrial complex IV deficiency, nuclear type 7
- mitochondrial complex IV deficiency, nuclear type 8
- mitochondrial complex IV deficiency, nuclear-type
- mitochondrial complex V (ATP synthase) deficiency, nuclear type 1
- mitochondrial complex V (ATP synthase) deficiency, nuclear type 2
- mitochondrial complex V (ATP synthase) deficiency, nuclear type 3
- mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A
- mitochondrial complex V (ATP synthase) deficiency, nuclear type 4B
- mitochondrial complex V (ATP synthase) deficiency, nuclear type 5
- mitochondrial complex V (ATP synthase) deficiency, nuclear type 7
- mitochondrial disease
- mitochondrial disease, non-human animal
- mitochondrial dna depletion syndrome 16B (neuroophthalmic type)
- mitochondrial dna depletion syndrome 21
- mitochondrial encephalomyopathy
- mitochondrial envelope
- mitochondrial fission encephalopathy, dog
- mitochondrial fission encephalopathy, non-human animal
- mitochondrial gene expression
- mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency
- mitochondrial import-stimulating factor
- mitochondrial inner membrane
- mitochondrial intermembrane space protein Tim12, yeast, homolog of
- mitochondrial matrix
- mitochondrial membrane
- mitochondrial membrane organization
- mitochondrial membrane transport disorder
- mitochondrial myopathy with a defect in mitochondrial-protein transport
- mitochondrial myopathy with diabetes
- mitochondrial myopathy with reversible cytochrome C oxidase deficiency
- mitochondrial myopathy, dog
- mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy
- mitochondrial myopathy, non-human animal
- mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome
- mitochondrial myopathy-lactic acidosis-deafness syndrome
- mitochondrial neurogastrointestinal encephalomyopathy
- mitochondrial non-syndromic sensorineural hearing loss
- mitochondrial nucleoid
- mitochondrial oxidative phosphorylation disorder
- mitochondrial promoter sequence-specific DNA binding
- mitochondrial protein import disorder
- mitochondrial protein processing
- mitochondrial protein-containing complex
- mitochondrial proton-transporting ATP synthase complex deficiency
- mitochondrial pyruvate carrier deficiency
- mitochondrial respiratory chain complex deficiency
- mitochondrial respiratory-chain inhibitor
- mitochondrial ribosome
