loading...| Preferred Name |
Leigh disease |
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| Synonyms |
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| Definitions |
Xref MGI. OMIM mapping confirmed by DO. [SN]. A mitochondrial metabolism 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. |
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| ID |
http://purl.obolibrary.org/obo/DOID_3652 |
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| comment |
Xref MGI. OMIM mapping confirmed by DO. [SN]. |
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| definition |
A mitochondrial metabolism 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. |
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| hasDbXref |
MESH:D007888 UMLS_CUI:C0023264 ORDO:506 ICD10CM:G31.82 OMIM:256000 SNOMEDCT_US_2016_03_01:29570005 OMIM:220111 NCI:C84814 |
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| hasExactSynonym |
juvenile subacute necrotizing encephalomyelopathy Infantile necrotizing encephalomyelopathy Leigh syndrome |
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| hasOBONamespace |
disease_ontology |
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| hasRelatedSynonym |
subacute necrotizing encephalomyelopathy |
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| id |
DOID:3652 |
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| imported from | ||
| inSubset | ||
| label |
Leigh disease |
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| prefixIRI |
DOID:3652 |
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| prefLabel |
Leigh disease |
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| subClassOf |
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