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Human disease

AttributesValues
rdf:type
owl:sameAs
description
  • Krankheit (de)
  • Human disease (en)
  • մարդու հիվանդություն (hy)
  • хвороба людини (uk)
  • مرض يصيب الإنسان (ar)
  • Malattia genetica (it)
  • genetički poremećaj (bs)
  • syndrom som huvudsakligen motsvarar en snabb tillväxt (sv)
exact match
exact match
health specialty
ICD-10
Mondo ID
Disease Ontology ID
Mondo ID
Disease Ontology ID
health specialty
ICD-10
  • Q87.3
Mondo ID
  • MONDO_0010193
Disease Ontology ID
  • DOID:14731
rdfs:label
  • Sindrome di Weaver (it)
  • Weaver syndrome (en)
  • Weaver-Syndrom (de)
  • Weaverin oireyhtymä (fi)
  • Weaverov sindrom (bs)
  • Weavers syndrom (sv)
  • Zespół Weavera (pl)
  • syndrome de Weaver (fr)
  • Синдром Уивера (ru)
  • متلازمة ويفر (ar)
  • ウィーバー症候群 (ja)
  • 韋弗綜合症 (zh)
skos:prefLabel
  • Sindrome di Weaver (it)
  • Weaver syndrome (en)
  • Weaver-Syndrom (de)
  • Weaverin oireyhtymä (fi)
  • Weaverov sindrom (bs)
  • Weavers syndrom (sv)
  • Zespół Weavera (pl)
  • syndrome de Weaver (fr)
  • Синдром Уивера (ru)
  • متلازمة ويفر (ar)
  • ウィーバー症候群 (ja)
  • 韋弗綜合症 (zh)
name
  • Sindrome di Weaver (it)
  • Weaver syndrome (en)
  • Weaver-Syndrom (de)
  • Weaverin oireyhtymä (fi)
  • Weaverov sindrom (bs)
  • Weavers syndrom (sv)
  • Zespół Weavera (pl)
  • syndrome de Weaver (fr)
  • Синдром Уивера (ru)
  • متلازمة ويفر (ar)
  • ウィーバー症候群 (ja)
  • 韋弗綜合症 (zh)
Freebase ID
Freebase ID
  • /m/02vnp1z
instance of
instance of
subclass of
subclass of
KEGG ID
KEGG ID
KEGG ID
  • H01751
UniProt disease ID
Orphanet ID
ICD-9-CM
genetic association
ICD-10-CM
GARD rare disease ID
OMIM ID
Genetics Home Reference Conditions ID
UniProt disease ID
  • DI-01141
Orphanet ID
  • 3447
ICD-9-CM
  • 759.89
genetic association
ICD-10-CM
  • Q87.3
GARD rare disease ID
  • 5545
  • 7878
OMIM ID
  • 277590
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