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Familial Temporal Lobe Epilepsy 5

Disease ID: disease_node_13371

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Dbxref	MIM:614417, ORDO:163717
Subclassof	DOID_0050736, DOID_0050737, DOID_3328
Data Source	DOID
Synonyms	ETL5
Doid Label	familial temporal lobe epilepsy 5
Doid Description	A temporal lobe epilepsy that has_material_basis_in heterozygous mutation in the CPA6 gene on chromosome 8q13.
Has Material Basis In	GENO_0000147, GENO_0000148
Disease Node Id	disease_node_13371
Doid Id	DOID_0060752
Label	Familial Temporal Lobe Epilepsy 5

Outgoing r'ship SUBCLASS_OF to/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Epilepsy, Temporal Lobe(ID:disease_node_2984) (Disease)

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