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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: Vascular Diseases (D014652)
Parent Node: Vasculitis (D014657)
..Starting node ..Arteritis (D001167)
Child Nodes:
........AIDS Arteritis, Central Nervous System (D020943)
........Endarteritis (D004692)
........Giant Cell Arteritis (D013700) 1
........Polyarteritis Nodosa (D010488) 1
........Takayasu Arteritis (D013625)
Sister Nodes:
..Aortitis (D001025)
..Arteritis (D001167) 7
..Behcet Syndrome (D001528)
..Cogan Syndrome (D055952) 2
..Malignant Atrophic Papulosis (D054853)
..Mucocutaneous Lymph Node Syndrome (D009080) 1
..Phlebitis (D010689) 3
..Purpura, Schoenlein-Henoch (D011695) 1
..Retinal Vasculitis (D031300) 1
..Shwartzman Phenomenon (D012790)
..Systemic Vasculitis (D056647) 9
..Thromboangiitis Obliterans (D013919)
..Vasculitis, Central Nervous System (D020293) 7
..Vasculitis, Leukocytoclastic, Cutaneous (D018366) 1
..Vasculitis, Lymphocytic, Cutaneous Small Vessel (C565222)
..Vasculitis, Lymphocytic, Nodular (C566008)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	890
Name:	Arteritis
Definition:	INFLAMMATION of any ARTERIES.
Alternative IDs:
ParentIDs:	MESH:D014652\|MESH:D014657
TreeNumbers:	C14.907.184 \|C14.907.940.090
Synonyms:	Arterial Inflammation \|Arteritides \|Inflammation, Arterial
Slim Mappings:	Cardiovascular disease
Reference:	MedGen: D001167 MeSH: D001167 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants