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human disease

AttributesValues
rdf:type
description
  • human disease (en)
  • Schilddrüsenerkrankung (de)
  • մարդու հիվանդություն (hy)
  • хвороба людини (uk)
  • مرض يصيب الإنسان (ar)
  • 病症 (zh)
exact match
Experimental Factor Ontology ID
health specialty
Mondo ID
Disease Ontology ID
Mondo ID
Experimental Factor Ontology ID
  • 1000827
health specialty
Mondo ID
  • MONDO_0006666
rdfs:label
  • Disgenesia tiroidea (it)
  • Kilpnäärme düsgenees (et)
  • dysgénésie thyroïdienne (fr)
  • thyroid dysgenesis (en)
  • خلل تكون الغدة الدرقية (ar)
  • 甲状腺发育不全 (zh)
skos:prefLabel
  • Disgenesia tiroidea (it)
  • Kilpnäärme düsgenees (et)
  • dysgénésie thyroïdienne (fr)
  • thyroid dysgenesis (en)
  • خلل تكون الغدة الدرقية (ar)
  • 甲状腺发育不全 (zh)
name
  • Disgenesia tiroidea (it)
  • Kilpnäärme düsgenees (et)
  • dysgénésie thyroïdienne (fr)
  • thyroid dysgenesis (en)
  • خلل تكون الغدة الدرقية (ar)
  • 甲状腺发育不全 (zh)
subclass of
subclass of
ICD-9-CM
ICD-10-CM
GARD rare disease ID
OMIM ID
ICD-9-CM
  • 246.8
ICD-10-CM
  • E03.4
GARD rare disease ID
  • 8426
OMIM ID
  • 218700
Human Phenotype Ontology ID
Human Phenotype Ontology ID
  • HP:0005990
  • HP:0008188
Commons category
Commons category
  • Thyroid dysgenesis
skos:altLabel
  • Hypoplasia of thyroid (disorder) (en)
  • Hypoplasia of thyroid (disorder) [Ambiguous] (en)
  • Thyroid Atrophy (en)
  • Thyroid Gland Atrophy (en)
  • Thyroid atrophy (disorder) (en)
  • atrophy of thyroid (en)
  • obsolete atrophy of thyroid (en)
OpenAlex ID
NCI Thesaurus ID
UMLS CUI
MeSH descriptor ID
on focus list of Wikimedia project
Microsoft Academic ID
MeSH tree code
MeSH descriptor ID
Microsoft Academic ID
MeSH tree code
OpenAlex ID
  • C2908839706
NCI Thesaurus ID
  • C26942
UMLS CUI
  • C0151516
  • C0749420
  • C1563716
MeSH descriptor ID
  • D050033
on focus list of Wikimedia project
Microsoft Academic ID
  • 2780648382
  • 2911047824
MeSH tree code
  • C16.131.894
  • C19.874.689
is owl:sameAs of
is about of
is subclass of of
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