Medical Subject Headings

Last uploaded: August 28, 2024
Preferred Name

Epilepsy, Rolandic
Synonyms

Centralopathic Epilepsy

Temporal-Central Focal Epilepsy

Epilepsy, Benign Rolandic

Benign Epilepsy Of Childhood With Centrotemporal Spikes

Centralopathic Epilepsies

Centrotemporal Epilepsy

Benign Childhood Epilepsy With Centro Temporal Spikes

Focal Epilepsy, Temporal-Central

Epilepsies, Centralopathic

Rolandic Epilepsies

Epilepsies, Rolandic

Benign Rolandic Epilepsy of Childhood

Sylvian Epilepsy

Focal Epilepsies, Temporal-Central

Epilepsy, Centrotemporal

Benign Rolandic Epilepsy

BCECTS

Epilepsy, Centralopathic

Epilepsy, Rolands

Rolandic Epilepsy

Temporal-Central Focal Epilepsies

Benign Epilepsy With Centrotemporal Spikes

Rolands Epilepsy

Epilepsies, Centrotemporal

Rolandic Epilepsy, Benign

Centrotemporal Epilepsies

Epilepsies, Temporal-Central Focal

Benign Childhood Epilepsy With Centro-Temporal Spikes

Epilepsy, Sylvian

BECTS

Epilepsy, Temporal-Central Focal

Temporal Central Focal Epilepsy

Definitions

An autosomal dominant inherited partial epilepsy syndrome with onset between age 3 and 13 years. Seizures are characterized by PARESTHESIA and tonic or clonic activity of the lower face associated with drooling and DYSARTHRIA. In most cases, affected children are neurologically and developmentally normal. (From Epilepsia 1998 39;Suppl 4:S32-S41)

ID

http://purl.bioontology.org/ontology/MESH/D019305

altLabel

Centralopathic Epilepsy

Temporal-Central Focal Epilepsy

Epilepsy, Benign Rolandic

Benign Epilepsy Of Childhood With Centrotemporal Spikes

Centralopathic Epilepsies

Centrotemporal Epilepsy

Benign Childhood Epilepsy With Centro Temporal Spikes

Focal Epilepsy, Temporal-Central

Epilepsies, Centralopathic

Rolandic Epilepsies

Epilepsies, Rolandic

Benign Rolandic Epilepsy of Childhood

Sylvian Epilepsy

Focal Epilepsies, Temporal-Central

Epilepsy, Centrotemporal

Benign Rolandic Epilepsy

BCECTS

Epilepsy, Centralopathic

Epilepsy, Rolands

Rolandic Epilepsy

Temporal-Central Focal Epilepsies

Benign Epilepsy With Centrotemporal Spikes

Rolands Epilepsy

Epilepsies, Centrotemporal

Rolandic Epilepsy, Benign

Centrotemporal Epilepsies

Epilepsies, Temporal-Central Focal

Benign Childhood Epilepsy With Centro-Temporal Spikes

Epilepsy, Sylvian

BECTS

Epilepsy, Temporal-Central Focal

Temporal Central Focal Epilepsy

AQL

BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI

cui

C0376532

C2363129

DC

1

definition

An autosomal dominant inherited partial epilepsy syndrome with onset between age 3 and 13 years. Seizures are characterized by PARESTHESIA and tonic or clonic activity of the lower face associated with drooling and DYSARTHRIA. In most cases, affected children are neurologically and developmentally normal. (From Epilepsia 1998 39;Suppl 4:S32-S41)

DX

19970101

HN

1997

Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000469

http://purl.bioontology.org/ontology/MESH/Q000151

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000401

Machine permutation

1997

Mapped from

http://purl.bioontology.org/ontology/MESH/C563392

http://purl.bioontology.org/ontology/MESH/C535499

http://purl.bioontology.org/ontology/MESH/C564467

MDA

19960613

MMR

20170224

MN

C10.228.140.490.360.280

C10.228.140.490.493.250

notation

D019305

prefLabel

Epilepsy, Rolandic

TERMUI

T729333

T812692

T368047

T368045

T812693

T368044

T057540

T368043

T717146

T368048

T368042

T686124

T057541

T812694

TH

NLM (1997)

OMIM (2013)

NLM (2009)

NLM (2000)

NLM (2008)

NLM (2010)

tui

T047

subClassOf

http://purl.bioontology.org/ontology/MESH/D000073376

http://purl.bioontology.org/ontology/MESH/D004828

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