Version: 8.0.0Date: Tue Jan 28 2025
Disease Genes: Trf (Mmu)
Disease
Source: DOID:9744
Definition: A diabetes mellitus that is characterized by destruction of pancreatic beta cells resulting in absent or extremely low insulin production.
Genes: Trf (Mmu)
Disease
Source: DOID:9970
Definition: An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness.
Genes: Trf (Mmu)
Disease
Source: DOID:10763
Definition: An artery disease characterized by chronic elevated blood pressure in the arteries.
Genes: Trf (Mmu)
Disease
Source: DOID:2355
Definition: A hematopoietic system disease that is characterized by a decrease in the normal number of red blood cells.
Genes: Trf (Mmu)
Disease
Source: DOID:11758
Definition: A microcytic anemia that is characterized by pallor, fatigue, lightheadedness, and weakness and has_material_basis_in low total body iron causing impaired synthesis of red blood cells.
Genes: Trf (Mmu)
Source: DOID:77
Definition: A disease of anatomical entity that is located_in the gastrointestinal tract.
Genes: Trf (Mmu)
Disease
Source: DOID:0050425
Definition: A central nervous system disease characterized by throbbing, pulling creeping or other unpleasant sensations in the legs and the irresistible urge to move them.
Genes: Trf (Mmu)
Disease
Source: DOID:2921
Definition: A nephritis that causes inflammation of the glomeruli located_in kidney.
Genes: Trf (Mmu)
Disease
Source: DOID:0050649
Definition: A metal metabolism disorder that is characterized by transferrin deficiency, microcytic anemia, and iron loading, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the structural gene for transferrin (TF) on chromosome 3q22.
Genes: Trf (Mmu)
Source: DOID:0060419
Definition: A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 3q29 region.
Genes: Trf (Mmu)