epilepsy in children
human disease
Facts
3 properties- Instance of
- class of disease
- Subclass of
- epilepsy, epilepsy syndrome[2][3]
- Genetic association
- KCNT1, GAL, ADORA2A, AP2M1, FRRS1L, CABP4, CACNA1A, CACNA1H, CHD2, CHRNA2, CHRNA4, CHRNB2, CRH, DNM1, GABRA1, GABRB3, GABRG2, GRIN2A, JRK, KCNMA1, LGI1, MAPK10, RELN, SCN1A, SCN3A, GLUT1, SLC6A1, SYNGAP1, NPRL3, CPA6, DEPDC5, CUX2, MICAL1, NPRL2, TBC1D24, NEXMIF, SRPX2[4][5][6][7][8][9][10][11][12][13][14][15][16][17]
🏷️ Also known as
en Childhood seizure
en epilepsy in children
ar الصرع عند الأطفال
ar الصرع عند الاطفال
fr épilepsie chez l'enfant
he אפילפסיה בילדים
hi बच्चों में मिर्गी
zh 兒童癲癇
zh 患有癫痫的儿童
zh 患有脑痫的儿童
zh-hant 患有癲癇的兒童
🔖 Identifiers · 11
- OpenAlex ID
- C2780145166, C3018325526
- Exact match
- www.orpha.net
- Freebase ID
- /m/0121l855
- ICD-10-CM
- G40.4
- MedlinePlus ID
- 007681
- Microsoft Academic ID (discontinued)
- 2780145166
- Mondo ID
- MONDO_0020072
- National Library of Latvia ID
- 000078772
- Orphanet ID
- 98259
- Raras disease ID
- D98259
🔗 Connections
Subclass of 1
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Summary
epilepsy in children is a class of disease[1].