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Leigh Disease

Disease ID: disease_node_4615

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DbxrefGARD:6877, ICD10CM:G31.82, MESH:D007888, MIM:256000, NCI:C84814, ORDO:506, SNOMEDCT_US_2023_03_01:29570005, UMLS_CUI:C0023264
SubclassofDOID_3762
Data SourceDOID, MESH
SynonymsInfantile necrotizing encephalomyelopathy, Leigh syndrome, juvenile subacute necrotizing encephalomyelopathy, subacute necrotizing encephalomyelopathy
Mesh IdD007888
Mesh LabelLeigh Disease
Mesh SubclassofD028361, D015323, D020739
Doid LabelLeigh disease
Doid DescriptionA cytochrome-c oxidase deficiency disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity. Xref MGI. OMIM mapping confirmed by DO. [SN].
Has SymptomSYMP_0000124, SYMP_0000654, SYMP_0000309, SYMP_0019145
Disease Node Iddisease_node_4615
Doid IdDOID_3652
LabelLeigh Disease