Decreased activity of mitochondrial respiratory chain
Symptom Information:
Symptom ID: | HPO:0008972 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of cell physiology(HPO:0011017) Abnormality of the mitochondrion(HPO:0012103) Abnormality of mitochondrial metabolism(HPO:0003287) Abnormal activity of mitochondrial respiratory chain(HPO:0011922) Decreased activity of mitochondrial respiratory chain(HPO:0008972) MedDRA: |
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Database Frequency: | 34 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Acyl-CoA dehydrogenase 9 deficiency | (Orphanet:99901) |
Alpers syndrome | (Orphanet:726) |
Autosomal recessive spastic ataxia with leukoencephalopathy | (Orphanet:314603) |
Autosomal recessive spastic paraplegia type 55 | (Orphanet:320375) |
Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
Behr syndrome | (Orphanet:1239) |
Combined oxidative phosphorylation defect type 11 | (Orphanet:324535) |
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
Combined oxidative phosphorylation defect type 17 | (Orphanet:369913) |
Combined oxidative phosphorylation defect type 8 | (Orphanet:319504) |
Combined oxidative phosphorylation defect type 9 | (Orphanet:319509) |
Congenital cataract - progressive muscular hypotonia - hearing loss - developmental delay | (Orphanet:330054) |
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Congenital lactic acidosis, Saguenay-Lac-St. Jean type | (Orphanet:70472) |
Fatal multiple mitochondrial dysfunction syndrome | (Orphanet:289573) |
GRACILE syndrome | (Orphanet:53693) |
Hypotonia with lactic acidemia and hyperammonemia | (Orphanet:137908) |
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency | (Orphanet:352563) |
Leber plus disease | (Orphanet:99718) |
Leigh syndrome with leukodystrophy | (Orphanet:255241) |
Leigh syndrome with nephrotic syndrome | (Orphanet:255249) |
Lethal infantile mitochondrial myopathy | (Orphanet:254857) |
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate | (Orphanet:314051) |
MERRF | (Orphanet:551) |
MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 | (OMIM:605711) |
MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 | (OMIM:614299) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria | (Orphanet:1933) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Mitochondrial DNA depletion syndrome, myopathic form | (Orphanet:254875) |
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency | (Orphanet:314637) |
NARP syndrome | (Orphanet:644) |
Navajo neurohepatopathy | (Orphanet:255229) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
Pontocerebellar hypoplasia type 6 | (Orphanet:166073) |