Mitochondrial Diseases

Disease ID: disease_node_10985

Connections displayed (default: 10).

Plants :

Formulations :

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Other Diseases :

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Dbxref	GARD:7048, MESH:D028361, SNOMEDCT_US_2023_03_01:240096000, UMLS_CUI:C0751651
Subclassof	DOID_655
Data Source	DOID, MESH
Mesh Id	D028361
Mesh Label	Mitochondrial Diseases
Mesh Subclassof	D008659
Doid Label	mitochondrial metabolism disease
Doid Description	An inherited metabolic disorder that involves mitochondrial metabolism dysfunction.
Disease Node Id	disease_node_10985
Doid Id	DOID_700
Label	Mitochondrial Diseases

Incoming r'ship SUBCLASS_OF to/from Pearson Syndrome(ID:disease_node_17024) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neurodevelopmental Disorder With Cardiomyopathy, Spasticity, And Brain Abnormalities(ID:disease_node_16833) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Short-Chain Enoyl-Coa Hydratase 1 Deficiency(ID:disease_node_16834) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Metabolism, Inborn Errors(ID:disease_node_5171) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Complex V (Atp Synthase) Deficiency(ID:disease_node_16791) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Pyruvate Carrier Deficiency(ID:disease_node_16811) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitochondrial Dna Depletion Syndrome(ID:disease_node_16818) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cytochrome-C Oxidase Deficiency(ID:disease_node_11065) (Disease)
Incoming r'ship SUBCLASS_OF to/from Coenzyme Q10 Deficiency Disease(ID:disease_node_17014) (Disease)
Incoming r'ship SUBCLASS_OF to/from Combined Oxidative Phosphorylation Deficiency(ID:disease_node_16714) (Disease)
Incoming r'ship SUBCLASS_OF to/from Adult-Onset Ataxia And Polyneuropathy(ID:disease_node_16790) (Disease)

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