(Q55787290)

English

familial partial epilepsy

instance of partial epilepsy that is caused by an inherited modification of the individual's genome

Epilepsy, partial, familial
hereditary partial epilepsy

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Statements

class of disease

0 references

channelopathy with epilepsy

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

adolescent-onset epilepsy syndrome

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Epilepsy in children

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

http://www.orpha.net/ORDO/Orphanet_309

0 references

Identifiers

GARD rare disease ID

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

based on heuristic

inferred by common Orphanet mappings on source and on Wikidata

16 June 2023

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Wiktionary(0 entries)

Multilingual sites(0 entries)

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