Version: 8.0.0Date: Tue Jan 28 2025
Disease Genes: Dmd (Mmu)
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: Dmd (Mmu)
Disease
Source: DOID:12930
Definition: An intrinsic cardiomyopathy that is characterized by an an enlarged heart and damage to the myocardium causing the heart to pump blood inefficiently.
Genes: Dmd (Mmu)
Disease
Source: DOID:1059
Definition: A specific developmental disorder that involves significant limitations both in mental functioning and in adaptive behavior such as communicating, taking care of him or herself, and social skills.
Genes: Dmd (Mmu)
Disease
Source: DOID:1561
Definition: A disease of mental health that affects cognitive functions including memory processing, perception and problem solving.
Genes: Dmd (Mmu)
Disease
Source: DOID:9884
Definition: A myopathy is characterized by progressive skeletal muscle weakness degeneration.
Genes: Dmd (Mmu)
Disease
Source: DOID:11723
Definition: A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy.
Genes: Dmd (Mmu)
Disease
Source: DOID:4724
Definition: A brain disease that is characterized by excess accumulation of fluid in the intracellular and/or extracellular spaces of the brain, has_symptom nausea, has_symptom vomiting, has_symptom blurred vision, has_symptom seizure, has_symptom coma.
Genes: Dmd (Mmu)
Disease
Source: DOID:9883
Definition: A muscular dystrophy that involves slowly worsening muscle weakness of the legs and pelvis, and has_material_basis_in X-linked recessive inheritance of mutation in the dystrophin gene on chromosome Xp21.
Genes: Dmd (Mmu)
Source: DOID:0110461
Definition: A dilated cardiomyopathy that has_material_basis_in mutation in the DMD gene encoding dystrophin on chromosome Xp21, without skeletal muscle weakness or wasting.
Genes: Dmd (Mmu)