About: adrenoleukodystrophy

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

MESH:D000326w added from NeuroDevNet [WAK].

Attributes	Values
type	Class
subClassOf	X-linked recessive disease leukodystrophy nodeID://b50947044
label	adrenoleukodystrophy
comment	MESH:D000326w added from NeuroDevNet [WAK].
has exact match	MESH:D000326
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:10588
has_alternative_id	DOID:13451
database_cross_reference	ICD10CM:E71.52 MESH:D000326 NCI:C61252 OMIM:300100 SNOMEDCT_US_2021_09_01:65389002 UMLS_CUI:C0162309
has_exact_synonym	ALD (en) Bronze Schilder disease (en) Encephalitis periaxialis concentrica (en) Encephalitis periaxialis, Schilder's (en) Siemerling-Creutzfeldt Disease (en) X-linked adrenoleukodystrophy (en) diffuse sclerosis (en) sudanophilic cerebral sclerosis (en)
has_obo_namespace	disease_ontology
in_subset	NCIthesaurus
http://purl.obolib...g/obo/IAO_0000115	A leukodystrophy that disrupts the breakdown of very-long-chain fatty acids resulting in progressive brain damage, failure of the adrenal glands and eventually death.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50947045

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