MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation 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

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: immune system disease (MONDO:0005046)
Parent Node: monkey disease (MONDO:0025102)
Parent Node: post-viral disorder (MONDO:0021674)
..Starting node ..simian acquired immunodeficiency syndrome ()
Child Nodes:
Sister Nodes:
..AIDS dementia complex ()
..AIDS-related disorder ()
..chronic Epstein-Barr virus infection syndrome ()
..hepatitis C induced liver cirrhosis ()
..hepatitis D ()
..herpes zoster ()
..oral hairy leukoplakia ()
..post-infectious neuralgia ()
..rubella encephalitis ()
..simian acquired immunodeficiency syndrome ()
..viral dilated cardiomyopathy ()
..virus associated tumor ()
..Zika virus congenital syndrome ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	25484
Name:	simian acquired immunodeficiency syndrome
Definition:	Acquired defect of cellular immunity that occurs naturally in macaques infected with srv serotypes, experimentally in monkeys inoculated with srv or mason-pfizer monkey virus; (mpmv), or in monkeys infected with simian immunodeficiency virus.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	AIDS, Simian; AIDSs, Simian; SAIDS; Simian acquired immune deficiency syndrome; Simian acquired immuno deficiency syndrome; Simian acquired immuno-deficiency syndrome; Simian AIDS; Simian AIDSs; Simian immunodeficiency virus caused monkey disease; Simian immunodeficiency virus monkey disease
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal