Version: 8.0.0Date: Tue Jan 28 2025
Disease Associated Species: Rattus norvegicus Genes: Cfh (Rno)
Disease
Source: DOID:0080600
Definition: A Coronavirus infectious disease that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2.
Genes: Cfh (Rno)
Disease
Source: DOID:8466
Definition: A retinal disease that is characterized by deterioration of the retina caused by the progressive and eventual death of the cells of the retina.
Genes: Cfh (Rno)
Disease
Source: DOID:9074
Definition: A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart.
Genes: Cfh (Rno)
Disease
Source: DOID:1686
Definition: An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function.
Genes: Cfh (Rno)
Disease
Source: DOID:8893
Definition: A skin disease that is characterized by patches of thick red skin and silvery scales.
Genes: Cfh (Rno)
Source: DOID:1287
Definition: A disease of anatomical entity which occurs in the blood, heart, blood vessels or the lymphatic system that passes nutrients (such as amino acids and electrolytes), gases, hormones, blood cells or lymph to and from cells in the body to help fight diseases and help stabilize body temperature and pH to maintain homeostasis.
Genes: Cfh (Rno)
Disease
Source: DOID:4448
Definition: A retinal degeneration characterized by gradual deterioration of light-sensing cells in the tissues at the back of the eye and has_symptom vision loss.
Genes: Cfh (Rno)
Disease
Source: DOID:0080162
Definition: A glomerulonephritis that is characterized by inflammation of the kidneys resulting from systemic lupus erythematosus.
Genes: Cfh (Rno)
Disease
Source: DOID:1749
Definition: A carcinoma that derives_from squamous epithelial cells.
Genes: Cfh (Rno)
Disease
Source: DOID:576
Definition: A kidney disease that is characterized by the presence of excess proteins in the urine.
Genes: Cfh (Rno)
Disease
Source: DOID:11335
Definition: A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs.
Genes: Cfh (Rno)
Disease
Source: DOID:2527
Definition: A proteinuria that is characterized by the leaking of blood protein into the urine, swelling or edema, and degenerative lesions without inflammation.
Genes: Cfh (Rno)
Disease
Source: DOID:670
Definition: A substance abuse that involves the recurring use of amphetamines despite negative consequences.
Genes: Cfh (Rno)
Disease
Source: DOID:12030
Definition: An uveitis that is characterized by inflammation of all layers of the uvea (middle layer) of the eye, which includes the iris, ciliary body, and choroid.
Genes: Cfh (Rno)
Source: DOID:0110017
Definition: An age related macular degeneration conferred by variation in the CFH gene on chromosome 1q31.
Genes: Cfh (Rno)
Disease
Source: DOID:0060746
Definition: A retinal drusen characterized by yellow-white deposits (drusen) that accumulate beneath the retinal pigment epithelium on Bruch membrane and that has_material_basis_in mutations in the CFH gene on chromosome 1q31.3.
Genes: Cfh (Rno)
Disease
Source: DOID:3454
Definition: A cerebrovascular disease that is characterized by tissue necrosis located_in the brain, resulting from inadequate blood flow through the brain.
Genes: Cfh (Rno)
Disease
Source: DOID:12554
Definition: A kidney disease that is characterized by hemolytic anemia, thrombocytopenia, and renal failure caused by platelet thrombi in the microcirculation of the kidney and other organs.
Genes: Cfh (Rno)
Source: DOID:2920
Definition: Not Available
Genes: Cfh (Rno)
Disease
Source: DOID:13603
Definition: A cholestasis characterized by yellowish pigmentation of the skin and sclera due to high bilirubin levels resulting from biliary tract obstruction.
Genes: Cfh (Rno)
Source: DOID:0080301
Definition: A complement deficiency that is characterized by mechanical hemolytic anemia, thrombocytopenia, and renal dysfunction.
Genes: Cfh (Rno)