About: polymicrogyria     Goto   Sponge   NotDistinct   Permalink

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A condition that affects the development of the human brain by multiple small gyri (microgyri) creating excessive folding of the brain leading to an abnormally thick cortex.

AttributesValues
rdf:type
owl:sameAs
description
  • Fehlbildung der Großhirnrinde (de)
  • حالة تؤثر على نمو الدماغ البشري نتيجة وجود العديد من التلافيف الصغيرة ما يؤدي إلى تشكل طيات مفرطة في الدماغ تزيد من سماكة القشرة المخية بشكل غير طبيعي (ar)
  • aangeboren hersenafwijking (nl)
  • A condition that affects the development of the human brain by multiple small gyri (microgyri) creating excessive folding of the brain leading to an abnormally thick cortex. (en)
exact match
exact match
health specialty
Mondo ID
DiseasesDB
Mondo ID
health specialty
Mondo ID
  • MONDO_0000087
DiseasesDB
  • 33975
rdfs:label
  • polymicrogyria (en)
  • Drobnozakrętowość (pl)
  • Polymikrogyrie (de)
  • polimicrogiria (es)
  • polimicrogíria (ca)
  • polymicrogyrie (fr)
  • polymicrogyrie (nl)
  • سندرم پریسیلویان (fa)
  • كثارة التلافيف (ar)
  • 多小腦迴畸形 (zh)
skos:prefLabel
  • polymicrogyria (en)
  • Drobnozakrętowość (pl)
  • Polymikrogyrie (de)
  • polimicrogiria (es)
  • polimicrogíria (ca)
  • polymicrogyrie (fr)
  • polymicrogyrie (nl)
  • سندرم پریسیلویان (fa)
  • كثارة التلافيف (ar)
  • 多小腦迴畸形 (zh)
name
  • polymicrogyria (en)
  • Drobnozakrętowość (pl)
  • Polymikrogyrie (de)
  • polimicrogiria (es)
  • polimicrogíria (ca)
  • polymicrogyrie (fr)
  • polymicrogyrie (nl)
  • سندرم پریسیلویان (fa)
  • كثارة التلافيف (ar)
  • 多小腦迴畸形 (zh)
Freebase ID
Freebase ID
  • /m/03v7qj
instance of
instance of
subclass of
subclass of
KEGG ID
KEGG ID
KEGG ID
  • H00271
Orphanet ID
ICD-10-CM
PatientsLikeMe condition ID
GARD rare disease ID
GeneReviews ID
Genetics Home Reference Conditions ID
Orphanet ID
  • 35981
ICD-10-CM
  • Q04.3
PatientsLikeMe condition ID
  • polymicrogyria
GARD rare disease ID
  • 12271
GeneReviews ID
  • NBK1329
Genetics Home Reference Conditions ID
  • polymicrogyria
Human Phenotype Ontology ID
ICD-9 ID
Human Phenotype Ontology ID
  • HP:0002126
ICD-9 ID
  • 742.2
Commons category
Commons category
  • Polymicrogyria
skos:altLabel
  • تكثر التلافيف الدماغية الدقيقة (ar)
  • polimicrogiria (ca)
  • كثرة التلافيف المكروية (ar)
OpenAlex ID
NCI Thesaurus ID
UMLS CUI
Quora topic ID
MeSH descriptor ID
Microsoft Academic ID
MeSH tree code
ICD-11 ID (MMS)
ICD-11 (foundation)
DeCS ID
MeSH descriptor ID
Microsoft Academic ID
MeSH tree code
OpenAlex ID
  • C2778596996
NCI Thesaurus ID
  • C116936
UMLS CUI
  • C0266464
Quora topic ID
  • Polymicrogyria
MeSH descriptor ID
  • D065706
Microsoft Academic ID
  • 2778596996
MeSH tree code
  • C10.500.507.500.500
  • C16.131.666.507.500.500
ICD-11 ID (MMS)
  • LA05.50
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