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Disease Browser
Parent Node: Seizures, Febrile (D003294)
..Starting node ..Febrile Convulsions, Familial, 10 (C567218)
Child Nodes:
Sister Nodes:
..Febrile Convulsions, Familial, 1 (C565162)
..Febrile Convulsions, Familial, 10 (C567218)
..Febrile Convulsions, Familial, 2 (C566541)
..Febrile Convulsions, Familial, 3a (C567820)
..Febrile Convulsions, Familial, 3b (C567821)
..Febrile Convulsions, Familial, 4 (C565788)
..Febrile Convulsions, Familial, 5 (C563762)
..Febrile Convulsions, Familial, 6 (C563764)
..Febrile Convulsions, Familial, 7 (C566929)
..Febrile Convulsions, Familial, 8 (C566975)
..Febrile Convulsions, Familial, 9 (C566901)
..Febrile Seizures Associated with Afebrile Seizures (C565813)
..Generalized Epilepsy with Febrile Seizures Plus (C565808)
..Generalized Epilepsy With Febrile Seizures Plus, 7 (C567827)
..Generalized Epilepsy With Febrile Seizures Plus, Type 1 (C565809)
..Generalized Epilepsy With Febrile Seizures Plus, Type 2 (C565810)
..Generalized Epilepsy With Febrile Seizures Plus, Type 3 (C565811)
..Generalized Epilepsy With Febrile Seizures Plus, Type 4 (C565227)
..Generalized Epilepsy With Febrile Seizures Plus, Type 5 (C565812)
..Generalized Epilepsy With Febrile Seizures Plus, Type 6 (C567371)
..GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 8 (OMIM:613828)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4210
Name:	Febrile Convulsions, Familial, 10
Definition:
Alternative IDs:	OMIM:612637
ParentIDs:	MESH:D003294
TreeNumbers:	C10.228.140.490.650/C567218
Synonyms:	CONVULSIONS, FAMILIAL FEBRILE, 10 \|FEB10 \|FEBRILE SEIZURES, FAMILIAL, 10 \|Seizures, Familial Febrile, 10
Slim Mappings:	Nervous system disease
Reference:	MedGen: C567218 MeSH: C567218 OMIM: 612637; Genes:
Phenotypes
Disease Causing ClinVar Variants