Disease Browser
Parent Node: Retinal Diseases (D012164) Parent Node: Vasculitis (D014657) ..Starting node .. Retinal Vasculitis (D031300) Child Nodes:
........Eales disease (C538011) 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: 9733
Name: Retinal Vasculitis
Definition: Inflammation of the retinal vasculature with various causes including infectious disease; LUPUS ERYTHEMATOSUS, SYSTEMIC; MULTIPLE SCLEROSIS; BEHCET SYNDROME; and CHORIORETINITIS.
Alternative IDs:
ParentIDs: MESH:D012164|MESH:D014657
TreeNumbers: C11.768.757 |C14.907.940.815
Synonyms: Vasculitis, Retinal
Slim Mappings: Cardiovascular disease|Eye disease
Reference:
MedGen: D031300
MeSH: D031300
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants