Mine sisu juurde

Alexander disease

Lehekülje sisu ei toetata teistes keeltes.

congenital disorder of nervous system

Välised allikad

Freebase
MeSH descriptor ID
D038261[2]

teema nimetus kujul: Alexander Disease

mapping relation type: täpne vaste

PatientsLikeMe condition ID
UniProt disease ID
DeCS ID
DiseasesDB
Gran Enciclopèdia Catalana ID
GeneReviews ID
Orphanet ID
58[2]

mapping relation type: täpne vaste

Disease Ontology ID
Gran Enciclopèdia Catalana ID (former scheme)
Genetics Home Reference Conditions ID
Mondo ID
Microsoft Academic ID
UMLS CUI
ICD-11 ID (MMS)
8A44.2

teema nimetus kujul: Alexander disease

GARD rare disease ID
ICD-11 (foundation)
ICD-10
ICD-10-CM
OMIM ID
KEGG ID
ICD-9 ID
MeSH tree code
WikiProjectMed ID

üksikjuht nähtusest

designated intractable/rare disease[4]
rare disease
class of disease

mille alamklass

leukodystrophy[5]
nervous system heredodegenerative disease[2]
eye degenerative disease[2]
autosomal dominant disease[5]

nimetatud ... järgi

William Stewart Alexander

meditsiiniline eriala

genetic association

external data available at URL

Wikimedia projekti fookusnimekiri

NCI Thesaurus ID

C84545[3]

Commonsi kategooria

Alexander disease

Viited

  1. Freebase Data Dumps, 28. oktoober 2013
  2. 2,0 2,1 2,2 2,3 2,4 2,5 Monarch Disease Ontology release 2018-06-29, 3. juuli 2018, MONDO_0008752
  3. 3,0 3,1 3,2 3,3 Disease Ontology, 15. mai 2019, DOID:4252
  4. 4,0 4,1 https://ddrare.nibiohn.go.jp/, 17. mai 2019
  5. 5,0 5,1 5,2 Disease Ontology, 29. november 2020, DOID:4252
  6. P14136, 13. august 2019, UniProt
  7. Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease
  8. Open Targets Platform, 24. august 2023, https://platform.opentargets.org/evidence/ENSG00000131095/MONDO_0008752, inferred from an Open Targets association score over 0.7
  9. Identifiers.org, https://registry.identifiers.org/registry/doid