Decreased activity of mitochondrial complex I
Symptom Information:
Symptom ID: | HPO:0011923 | ||
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) Decreased activity of mitochondrial complex I(HPO:0011923) MedDRA: |
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Database Frequency: | 35 / 7739 | ||
Resource: |
All diseases associated with this symptom:
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) |
Cardiomyopathy, dilated, 1GG | (OMIM:613642) |
Combined oxidative phosphorylation defect type 11 | (Orphanet:324535) |
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
Combined oxidative phosphorylation defect type 17 | (Orphanet:369913) |
Combined oxidative phosphorylation defect type 2 | (Orphanet:254920) |
Combined oxidative phosphorylation defect type 4 | (Orphanet:254925) |
Combined oxidative phosphorylation defect type 7 | (Orphanet:254930) |
Combined oxidative phosphorylation defect type 8 | (Orphanet:319504) |
Combined oxidative phosphorylation defect type 9 | (Orphanet:319509) |
Combined oxidative phosphorylation deficiency type 23 | (ORPHA:444013) |
Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency | (Orphanet:289527) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 | (Orphanet:137681) |
Hereditary myopathy with lactic acidosis due to ISCU deficiency | (Orphanet:43115) |
Histiocytoid cardiomyopathy | (Orphanet:137675) |
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome | (Orphanet:363694) |
Hypotonia with lactic acidemia and hyperammonemia | (Orphanet:137908) |
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency | (Orphanet:352563) |
Leber plus disease | (Orphanet:99718) |
Lethal infantile mitochondrial myopathy | (Orphanet:254857) |
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate | (Orphanet:314051) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 | (OMIM:600462) |
Myopathy, lactic acidosis, and sideroblastic anemia 2; MLASA2 | (OMIM:613561) |
NARP syndrome | (Orphanet:644) |
Navajo neurohepatopathy | (Orphanet:255229) |
Nephronophthisis-like nephropathy 1 | (OMIM:613159) |
Pontocerebellar hypoplasia type 6 | (Orphanet:166073) |
Pyruvate dehydrogenase lipoic acid synthetase deficiency | (OMIM:614462) |
Pyruvate dehydrogenase phosphatase deficiency | (Orphanet:79246) |