- Autosomal hereditary disorder
- 常染色体遗传病症
Medical Chinese dictionary (湘雅医学词典). 2013.
Autosomal hereditary disorder
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autosomal dominant disorder — noun a disease caused by a dominant mutant gene on an autosome • Syn: ↑autosomal dominant disease • Hypernyms: ↑genetic disease, ↑genetic disorder, ↑genetic abnormality, ↑genetic defect, ↑congenital disease, ↑ … Useful english dictionary
Hereditary multiple exostoses — Classification and external resources Photograph of the legs of a 26 year old male showing multiple lumps leading to deformity. ICD 10 Q … Wikipedia
Hereditary sensory and autonomic neuropathy — For the gene HSN2, see HSN2. Not to be confused with Hereditary motor and sensory neuropathy. Hereditary sensory and autonomic neuropathy Classification and external resources ICD 9 356.2 OMIM … Wikipedia
hereditary condition — noun a disease or disorder that is inherited genetically • Syn: ↑genetic disease, ↑genetic disorder, ↑genetic abnormality, ↑genetic defect, ↑congenital disease, ↑inherited disease, ↑inherited disorder, ↑ … Useful english dictionary
hereditary disease — noun a disease or disorder that is inherited genetically • Syn: ↑genetic disease, ↑genetic disorder, ↑genetic abnormality, ↑genetic defect, ↑congenital disease, ↑inherited disease, ↑inherited disorder, ↑ … Useful english dictionary
autosomal dominant disease — noun a disease caused by a dominant mutant gene on an autosome • Syn: ↑autosomal dominant disorder • Hypernyms: ↑genetic disease, ↑genetic disorder, ↑genetic abnormality, ↑genetic defect, ↑congenital disease, ↑ … Useful english dictionary
Hereditary angioedema — A genetic form of angioedema. (Angioedema is also referred to as Quinke’s disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to… … Medical dictionary
hereditary progressive arthro-ophthalmopathy — an autosomal dominant disorder consisting of myopia progressing to retinal detachment and blindness, and premature degenerative changes in the joints; sensorineural deafness may also occur. Called also Stickler syndrome … Medical dictionary
hereditary benign intraepithelial dyskeratosis — an autosomal dominant disorder caused by mutation at 4q35, characterized by foamy gelatinous plaques on the conjunctiva and white thickenings resembling leukoplakia on the oral mucosa; photophobia is common in children, and blindness may occur.… … Medical dictionary
Hereditary elliptocytosis — Classification and external resources Blood smear showing elliptocytes ICD 10 D … Wikipedia
Hereditary inclusion body myopathy — Hereditary inclusion body myopathies (HIBM) are a heterogeneous group of genetic disorders which have different symptoms. Generally, they are neuromuscular disorders characterized by muscle weakness developing in young adults. Hereditary… … Wikipedia
