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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: Brain Diseases (D001927)
Parent Node: Craniocerebral Trauma (D006259)
..Starting node ..Brain Injuries (D001930)
Child Nodes:
........Brain Concussion (D001924) 2
........Brain Hemorrhage, Traumatic (D020201) 2
........Brain Injury, Chronic (D020208)
........Diffuse Axonal Injury (D020833)
........Epilepsy, Post-Traumatic (D004834)
........Pneumocephalus (D011007)
........Shaken Baby Syndrome (D038642)
Sister Nodes:
..Brain Injuries (D001930) 11
..Cerebrospinal Fluid Leak (D065634) 2
..Coma, Post-Head Injury (D020207)
..Cranial Nerve Injuries (D020209) 15
..Facial Injuries (D005151) 15
..Head Injuries, Closed (D016489) 3
..Head Injuries, Penetrating (D020197)
..Intracranial Hemorrhage, Traumatic (D020198) 10
..Skull Fractures (D012887) 7
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1452
Name:	Brain Injuries
Definition:	Acute and chronic (see also BRAIN INJURIES, CHRONIC) injuries to the brain, including the cerebral hemispheres, CEREBELLUM, and BRAIN STEM. Clinical manifestations depend on the nature of injury. Diffuse trauma to the brain is frequently associated with DIFFUSE AXONAL INJURY or COMA, POST-TRAUMATIC. Localized injuries may be associated with NEUROBEHAVIORAL MANIFESTATIONS; HEMIPARESIS, or other focal neurologic deficits.
Alternative IDs:
ParentIDs:	MESH:D001927\|MESH:D006259
TreeNumbers:	C10.228.140.199 \|C10.900.300.087 \|C26.260.118 \|C26.915.300.200
Synonyms:	Acute Brain Injuries \|Acute Brain Injury \|Brain Contusion \|Brain Contusions \|Brain Injuries, Acute \|Brain Injuries, Diffuse \|Brain Injuries, Focal \|Brain Injuries, Traumatic \|Brain Injury \|Brain Injury, Acute \|Brain Injury, Diffuse \|Brain Injury, Focal \|Brain Injury
Slim Mappings:	Nervous system disease\|Wounds and injuries
Reference:	MedGen: D001930 MeSH: D001930 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants