X-linked adrenoleukodystrophy (X-ALD) is a peroxisomal disorder resulting in cerebral demyelination, axonal dysfunction in the spinal cord leading to spastic paraplegia, adrenal insufficiency and in some cases testicular insufficiency. [ Orphanet:43 ]

This is just here as a test because I lose it

Term information

database cross reference
  • ICD10:E71.529 (DOID:10588)
  • MESH:D000326 (Orphanet:43)
  • MedDRA:10051260 (Orphanet:43)
  • ICD9:341.1 (MONDO:relatedTo)
  • DOID:10588 (MONDO:equivalentTo)
  • GARD:0005758 (Orphanet-shared)
  • ICD10:E71.3 (Orphanet:43)
  • Orphanet:43 (MONDO:equivalentTo)
  • ICD10:E71.52 (DOID:10588)
  • NCIT:C61252 (MONDO:equivalentTo)
  • ICD10:G37.0 (DOID:10588)
Subsets

ordo_disease

closeMatch

http://identifiers.org/snomedct/192932009

http://purl.obolibrary.org/obo/NCIT_C84670

http://identifiers.org/snomedct/44875002

http://identifiers.org/snomedct/267702006

http://identifiers.org/snomedct/155059003

definition

X-linked adrenoleukodystrophy (X-ALD) is a peroxisomal disorder resulting in cerebral demyelination, axonal dysfunction in the spinal cord leading to spastic paraplegia, adrenal insufficiency and in some cases testicular insufficiency.

exactMatch

http://www.orpha.net/ORDO/Orphanet_43

http://linkedlifedata.com/resource/umls/id/C0162309

http://identifiers.org/meddra/10051260

http://purl.obolibrary.org/obo/DOID_10588

http://purl.obolibrary.org/obo/NCIT_C61252

http://identifiers.org/mesh/D000326

excluded from QC check

http://purl.obolibrary.org/obo/mondo/sparql/single-child-tags.sparql

has exact synonym

Schilder's disease

diffuse sclerosis

Siemerling-Creutzfeldt disease

sudanophilic cerebral sclerosis

encephalitis periaxialis concentrica

X-linked adrenoleukodystrophy

Bronze-Schilder disease

X-ALD

adrenoleukodystrophy, X-linked

Schilder disease

X-linked ALD

diffuse cerebral sclerosis of Schilder

encephalitis periaxialis, Schilder's

ALD

has related synonym

adrenoleukodystrophy

id

MONDO:0018544