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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: Angiomatosis (D000798)
Parent Node: Bartonella Infections (D001474)
Parent Node: Skin Diseases, Bacterial (D017192)
Parent Node: Skin Diseases, Vascular (D017445)
..Starting node ..Angiomatosis, Bacillary (D016917)
Child Nodes:
Sister Nodes:
..Angioma serpiginosum, autosomal dominant (C536365)
..Angioma serpiginosum, X-linked (C536366)
..Angiomatosis, Bacillary (D016917)
..Behcet Syndrome (D001528)
..Cutis marmorata telangiectatica congenita (C536226)
..Gardner-Diamond syndrome (C535645)
..Giant Cell Arteritis (D013700) 1
..Livedo Reticularis (D054068) 1
..Malignant Atrophic Papulosis (D054853)
..Megalencephaly cutis marmorata telangiectatica congenita (C536142)
..Mucocutaneous Lymph Node Syndrome (D009080) 1
..Polyarteritis Nodosa (D010488) 1
..Pyoderma Gangrenosum (D017511) 1
..Sneddon Syndrome (D018860)
..Takayasu Arteritis (D013625)
..Urticaria (D014581) 12
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	695
Name:	Angiomatosis, Bacillary
Definition:	A reactive vascular proliferation that is characterized by the multiple tumor-like lesions in skin, bone, brain, and other organs. Bacillary angiomatosis is caused by infection with gram-negative Bartonella bacilli (such as BARTONELLA HENSELAE), and is often seen in AIDS patients and other IMMUNOCOMPROMISED HOSTS.
Alternative IDs:
ParentIDs:	MESH:D000798\|MESH:D001474\|MESH:D017192\|MESH:D017445
TreeNumbers:	C01.252.400.126.100.050 \|C01.252.825.150 \|C01.539.800.720.150 \|C14.907.077.060 \|C17.800.838.765.150 \|C17.800.862.060
Synonyms:	Angiomatoses, Bacillary \|Angiomatoses, Bacillary Epithelioid \|Angiomatoses, Epithelioid \|Angiomatosis, Bacillary Epithelioid \|Angiomatosis, Epithelioid \|Bacillary Angiomatoses \|Bacillary Angiomatosis \|Bacillary Epithelioid Angiomatoses \|Bacillary Epithelioid Ang
Slim Mappings:	Bacterial infection or mycosis\|Cardiovascular disease\|Skin disease
Reference:	MedGen: D016917 MeSH: D016917 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants