About: Leigh disease

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An Entity of Type : owl:Class, within Data Space : demo.openlinksw.com associated with source document(s)

Xref MGI. OMIM mapping confirmed by DO. [SN].

Attributes	Values
type	Class
subClassOf	mitochondrial metabolism disease nodeID://b50952164 nodeID://b50952165 nodeID://b50952166 nodeID://b50952167
label	Leigh disease
comment	Xref MGI. OMIM mapping confirmed by DO. [SN].
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:3652
database_cross_reference	GARD:6877 ICD10CM:G31.82 MESH:D007888 NCI:C84814 OMIM:256000 ORDO:506 SNOMEDCT_US_2021_09_01:29570005 UMLS_CUI:C0023264
has_exact_synonym	Infantile necrotizing encephalomyelopathy (en) Leigh syndrome (en) juvenile subacute necrotizing encephalomyelopathy (en)
has_obo_namespace	disease_ontology
has_related_synonym	subacute necrotizing encephalomyelopathy (en)
in_subset	DO_FlyBase_slim DO_rare_slim NCIthesaurus
http://purl.obolib...g/obo/IAO_0000115	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.
is subClassOf of	French Canadian Leigh disease
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50952168

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