Version: 8.0.0Date: Tue Jan 28 2025
Disease Genes: Hspa1b (Mmu)
Disease
Source: DOID:10652
Definition: A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.
Genes: Hspa1b (Mmu)
Disease
Source: DOID:9352
Definition: A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.
Genes: Hspa1b (Mmu)
Disease
Source: DOID:5419
Definition: A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness.
Genes: Hspa1b (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: Hspa1b (Mmu)
Disease
Source: DOID:14115
Definition: A commensal bacterial infectious disease that results_in infection, has_material_basis_in Streptococcus pyogenes or has_material_basis_in Staphylococcus aureus, which produce toxins that are absorbed systemically and produce the systemic manifestations. The infection has_symptom fever, has_symptom rash, has_symptom hypotension, has_symptom multiorgan failure, has_symptom desquamation, has_symptom vomiting, has_symptom diarrhea, has_symptom headache, and has_symptom nonfocal neurologic abnormalities.
Genes: Hspa1b (Mmu)
Disease
Source: DOID:0080205
Definition: A urinary system disease characterized by structural malformations in the kidney and/or urinary tract containing vesicoureteral reflux.
Genes: Hspa1b (Mmu)
Disease
Source: DOID:9669
Definition: A cataract that is characterized by thickening and loss of transparency of the lens with age progression, caused by a multifactorial etiology related to aging.
Genes: Hspa1b (Mmu)
Disease
Source: DOID:2316
Definition: An ischemia that is characterized by insufficient blood flow to the brain to meet metabolic demand.
Genes: Hspa1b (Mmu)
Disease
Source: DOID:0081267
Definition: An immune system disease that is characterized by recognition by mature donor T cells, that contaminate the allogeneic bone marrow, of the recipient's tissue as foreign, causing a severe inflammatory disease characterized by rashes, diarrhea, and liver disease, and that has_material_basis_in an associated with variation in the interleukin-10 gene (IL10) on chromosome 1q32.
Genes: Hspa1b (Mmu)
Disease
Source: DOID:0080784
Definition: An urinary system disease that is characterized by an infection in any part of the urinary system, including the kidneys, ureters, bladder or urethra.
Genes: Hspa1b (Mmu)