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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 Injuries (D001930)
Parent Node: Central Nervous System Diseases (D002493)
..Starting node ..Pneumocephalus (D011007)
Child Nodes:
Sister Nodes:
..Brain Diseases (D001927) 1149
..Central Nervous System Infections (D002494) 96
..Encephalomyelitis (D004679) 8
..Endocrine-Cerebroosteodysplasia (C567210)
..Flynn Aird syndrome (C537066)
..High Pressure Neurological Syndrome (D006610)
..Meningitis (D008581) 19
..Movement Disorders (D009069) 306
..Neurosarcoidosis (C535814)
..Ocular Motility Disorders (D015835) 109
..Pneumocephalus (D011007)
..Renal cysts and diabetes syndrome (C535520)
..Skeletal Dysplasia And Progressive Central Nervous System Degeneration, Lethal (C566514)
..Spinal Cord Diseases (D013118) 170
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9018
Name:	Pneumocephalus
Definition:	Presence of air or gas within the intracranial cavity (e.g., epidural space, subdural space, intracerebral, etc.) which may result from traumatic injuries, fistulous tract formation, erosions of the skull from NEOPLASMS or infection, NEUROSURGICAL PROCEDURES, and other conditions.
Alternative IDs:
ParentIDs:	MESH:D001930\|MESH:D002493
TreeNumbers:	C10.228.140.199.700 \|C10.228.806 \|C10.900.300.087.700 \|C26.260.118.650 \|C26.915.300.200.650
Synonyms:	Airocele, Cranial \|Airoceles, Cranial \|Cranial Airocele \|Cranial Airoceles \|Cranial Pneumocyst \|Cranial Pneumocysts \|Epidural Pneumocephalus \|Gas, Intracranial \|Intracranial Gas \|Pneumocephalus, Epidural \|Pneumocephalus, Pressure \|Pneumocephalus, Tension \|Pneumoceph
Slim Mappings:	Nervous system disease\|Wounds and injuries
Reference:	MedGen: D011007 MeSH: D011007 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants