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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Epilepsies, Partial (D004828)
..Starting node ..Epilepsy, Partial, Sensory (D020937)
Child Nodes:
........Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease (C565928)
Sister Nodes:
..Cortical Dysplasia-Focal Epilepsy Syndrome (C566482)
..Epilepsy, Complex Partial (D017029)
..Epilepsy, Frontal Lobe (D017034) 6
..Epilepsy, Partial, Motor (D020938)
..Epilepsy, Partial, Sensory (D020937) 1
..Epilepsy, Partial, with Pericentral Spikes (C564605)
..Epilepsy, Partial, with Variable Foci (C565785)
..Epilepsy, Rolandic (D019305) 3
..Epilepsy, Temporal Lobe (D004833) 6
..Pitt-Hopkins-Like Syndrome 1 (C567657)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	3884
Name:	Epilepsy, Partial, Sensory
Definition:	A disorder characterized by recurrent focal onset seizures which have sensory (i.e., olfactory, visual, tactile, gustatory, or auditory) manifestations. Partial seizures that feature alterations of consciousness are referred to as complex partial seizures (EPILEPSY, COMPLEX PARTIAL).
Alternative IDs:
ParentIDs:	MESH:D004828
TreeNumbers:	C10.228.140.490.360.275
Synonyms:	Epilepsy, Sensory \|Epilepsy, Sensory Partial \|Focal Seizure Disorder, Sensory \|Focal Sensory Seizure \|Focal Sensory Seizures \|Gustatory Partial Seizure \|Gustatory Partial Seizures \|Olfactory Partial Seizure \|Olfactory Partial Seizures \|Partial Epilepsy, Sensory \|P
Slim Mappings:	Nervous system disease
Reference:	MedGen: D020937 MeSH: D020937 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants