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Netherton syndrome

Lehekülje sisu ei toetata teistes keeltes.

Human disease

Välised allikad

WikiProjectMed ID
Genetics Home Reference Conditions ID
SNOMED CT ID
MeSH tree code
DiseasesDB
Microsoft Academic ID
eMedicine ID
KEGG ID
UMLS CUI
C0265962[2]

mapping relation type: close match

BabelNet ID
GARD rare disease ID
UniProt disease ID
MeSH descriptor ID
D056770[2]

teema nimetus kujul: Netherton Syndrome

mapping relation type: täpne vaste

ICD-10
ICD-11 (foundation)
OMIM ID
256500[2]

mapping relation type: täpne vaste

ICD-10-CM
ICD-9 ID
Orphanet ID
634[2]

mapping relation type: täpne vaste

Medical Dictionary for Regulatory Activities ID
Disease Ontology ID
Mondo ID

üksikjuht nähtusest

rare disease
class of disease

mille alamklass

autosomal recessive disease[6]
ihtüoos
skin disease[6]

meditsiiniline eriala

medical genetics

sümptomid

Trichorrhexis invaginata

genetic association

Wikimedia projekti fookusnimekiri

NCI Thesaurus ID

C84922[2]

mapping relation type: täpne vaste

Viited

  1. 1,0 1,1 1,2 1,3 Disease Ontology, 28. august 2019, DOID:0050474
  2. 2,0 2,1 2,2 2,3 2,4 2,5 2,6 Monarch Disease Ontology release 2018-06-29, 6. august 2018, MONDO_0009735
  3. UMLS 2023, 25. mai 2023, inferred by common MeSH mappings on source and on Wikidata
  4. BabelNet
  5. inferred by common ICD-10 mappings on Wikidata and on source, https://cdn.who.int/media/docs/default-source/classification/icd/icd-10/icd-10-to-meddra-map---june-2023---codes-mapping.xlsx
  6. 6,0 6,1 6,2 6,3 Disease Ontology, 23. november 2021, DOID:0050474
  7. Disease Ontology, 30. november 2020, DOID:0050474
  8. Q9NQ38, 13. august 2019, UniProt
  9. Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome
  10. Open Targets Platform, 24. august 2023, https://platform.opentargets.org/evidence/ENSG00000133710/MONDO_0009735, inferred from an Open Targets association score over 0.7
  11. Identifiers.org, https://registry.identifiers.org/registry/doid