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: angiomatosis (MONDO:0024461)
Parent Node: bartonellosis (MONDO:0005664)
Parent Node: benign neoplasm of skin (MONDO:0021440)
Parent Node: skin disease caused by bacterial infection (MONDO:0024295)
..Starting node ..bacillary angiomatosis ()
Child Nodes:
Sister Nodes:
..aquarium granuloma ()
..bacillary angiomatosis ()
..bacterial exanthem ()
..bullous impetigo ()
..cellulitis (disease) ()
..cutaneous anthrax ()
..cutaneous syphilis ()
..cutaneous tuberculosis ()
..digital dermatitis in cattle ()
..erysipelas ()
..gas gangrene ()
..gonococcal keratitis ()
..impetigo ()
..pinta disease ()
..Ritter disease ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	758
Name:	bacillary angiomatosis
Definition:	A condition that is caused by infection with Bartonella, and which is characterized by vascular proliferation, usually in immunocompromised individuals.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	angiomatoses, bacillary; angiomatoses, bacillary epithelioid; angiomatoses, epithelioid; angiomatosis, bacillary epithelioid; angiomatosis, epithelioid; bacillary Angiomatoses; bacillary angiomatosis; bacillary epithelioid Angiomatoses; bacillary epithelioid angiomatosis; Bartonella angiomatosis; Ba
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal