- osteogenesis imperfecta [DOID:12347]
An osteochondrodysplasia that has_material_basis_in a deficiency in type-I collagen which results_in brittle bones and defective connective tissue.
- nuclear type mitochondrial complex I deficiency 20 [DOID:0112072]
A nuclear type mitochondrial complex I deficiency characterized by infantile onset of acute metabolic acidosis, hypertrophic cardiomyopathy, and muscle weakness associated with deficiency of mitochondrial complex I activity in muscle, liver, and fibroblasts that has_material_basis_in homozygous or compound heterozygous mutation in the ACAD9 gene on chromosome 3q21.3.
- food allergy [DOID:3044]
A hypersensitivity reaction type I disease that is an abnormal response to a food, triggered by the body's immune system.