polymicrogyria
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
Facts
6 properties
🏷️ Also known as
en polymicrogyria
en PMG
ar كثرة التلافيف المكروية
ar تكثر التلافيف الدماغية الدقيقة
ar كثارة التلافيف
de Polymikrogyrie
es polimicrogiria
fa سندرم پریسیلویان
fr polymicrogyrie
pl Drobnozakrętowość
zh 多小腦迴畸形
🔖 Identifiers · 24
- OpenAlex ID
- C2778596996
- DeCS ID
- 55574
- DiseasesDB
- 33975
- Exact match
- purl.obolibrary.org
- Freebase ID
- /m/03v7qj
- GARD rare disease ID
- 12271
- GeneReviews ID
- NBK1329
- Genetics Home Reference Conditions ID
- polymicrogyria
- Human Phenotype Ontology ID
- HP:0002126
- ICD-10-CM
- Q04.3
- ICD-11 ID (Foundation)
- 2081858551
- ICD-11 ID (MMS)
- LA05.50
Show all 24 identifiers +12
- ICD-9 ID
- 742.2
- KEGG ID
- H00271
- MeSH descriptor ID
- D065706
- MeSH tree code
- C10.500.507.500.500, C16.131.666.507.500.500
- Microsoft Academic ID (discontinued)
- 2778596996
- Mondo ID
- MONDO_0000087
- Orphanet ID
- 35981
- PatientsLikeMe condition ID
- polymicrogyria
- Quora topic ID
- Polymicrogyria
- Raras disease ID
- D35981
- UMLS CUI
- C0266464
- WikiProjectMed ID
- Polymicrogyria
🔗 Connections
Health specialty 1
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Summary
polymicrogyria is a class of disease[1].