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form of arteriopathy

AttributesValues
rdf:type
description
  • Krankheit (de)
  • maladie (fr)
  • مرض يصيب الإنسان (ar)
  • хвороба (uk)
  • form of arteriopathy (en)
exact match
exact match
Experimental Factor Ontology ID
health specialty
ICD-10
Mondo ID
DiseasesDB
Disease Ontology ID
Mondo ID
Disease Ontology ID
Experimental Factor Ontology ID
  • 1001186
health specialty
ICD-10
  • M30.8
Mondo ID
  • MONDO_0008436
DiseasesDB
  • 12257
Disease Ontology ID
  • DOID:13096
rdfs:label
  • Sneddon syndrome (en)
  • Sneddon's syndrome (en-ca)
  • Sneddon's syndrome (en-gb)
  • Sneddon-Syndrom (de)
  • Sneddons syndrom (da)
  • Sneddon综合征 (zh)
  • Sneddon综合征 (zh-cn)
  • Síndrome de Sneddon (gl)
  • Zespół Sneddona (pl)
  • syndrome de Sneddon (fr)
  • синдром снеддона (ru)
  • متلازمة سنيدون (ar)
skos:prefLabel
  • Sneddon syndrome (en)
  • Sneddon's syndrome (en-ca)
  • Sneddon's syndrome (en-gb)
  • Sneddon-Syndrom (de)
  • Sneddons syndrom (da)
  • Sneddon综合征 (zh)
  • Sneddon综合征 (zh-cn)
  • Síndrome de Sneddon (gl)
  • Zespół Sneddona (pl)
  • syndrome de Sneddon (fr)
  • синдром снеддона (ru)
  • متلازمة سنيدون (ar)
name
  • Sneddon syndrome (en)
  • Sneddon's syndrome (en-ca)
  • Sneddon's syndrome (en-gb)
  • Sneddon-Syndrom (de)
  • Sneddons syndrom (da)
  • Sneddon综合征 (zh)
  • Sneddon综合征 (zh-cn)
  • Síndrome de Sneddon (gl)
  • Zespół Sneddona (pl)
  • syndrome de Sneddon (fr)
  • синдром снеддона (ru)
  • متلازمة سنيدون (ar)
instance of
instance of
subclass of
subclass of
UniProt disease ID
Orphanet ID
genetic association
ICD-10-CM
PatientsLikeMe condition ID
GARD rare disease ID
OMIM ID
UniProt disease ID
  • DI-04206
Orphanet ID
  • 820
genetic association
ICD-10-CM
  • I77.8
PatientsLikeMe condition ID
  • sneddon-s-syndrome
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