Disease browser and phenotype portal

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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: Dementia (D003704)
Parent Node: HIV Infections (D015658)
..Starting node ..AIDS Dementia Complex (D015526)
Child Nodes:
Sister Nodes:
..Acquired Immunodeficiency Syndrome (D000163)
..AIDS Arteritis, Central Nervous System (D020943)
..AIDS Dementia Complex (D015526)
..AIDS-Associated Nephropathy (D016263)
..AIDS-Related Complex (D000386)
..AIDS-Related Opportunistic Infections (D017088) 1
..Coronary Artery Disease, Development of, in HIV (C563569)
..HIV Enteropathy (D019053)
..HIV Seropositivity (D006679)
..HIV Wasting Syndrome (D019247)
..HIV-Associated Lipodystrophy Syndrome (D039682)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	380
Name:	AIDS Dementia Complex
Definition:	A neurologic condition associated with the ACQUIRED IMMUNODEFICIENCY SYNDROME and characterized by impaired concentration and memory, slowness of hand movements, ATAXIA, incontinence, apathy, and gait difficulties associated with HIV-1 viral infection of the central nervous system. Pathologic examination of the brain reveals white matter rarefaction, perivascular infiltrates of lymphocytes, foamy macrophages, and multinucleated giant cells. (From Adams et al., Principles of Neurology, 6th ed, pp760-1; N Engl J Med, 1995 Apr 6;332(14):934-40)
Alternative IDs:
ParentIDs:	MESH:D003704\|MESH:D015658
TreeNumbers:	C02.782.815.616.400.070 \|C02.800.801.400.070 \|C10.228.140.380.070 \|C20.673.480.070 \|F03.087.400.050
Synonyms:	Acquired-Immune Deficiency Syndrome Dementia Complex \|AIDS Encephalopathies \|AIDS Encephalopathy \|AIDS Related Dementia Complex \|AIDS-Related Dementia Complex \|Complex, AIDS Dementia \|Complex, AIDS-Related Dementia \|Dementia Complex, Acquired Immune Deficiency
Slim Mappings:	Immune system disease\|Mental disorder\|Nervous system disease\|Viral disease
Reference:	MedGen: D015526 MeSH: D015526 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants