- autosomal hereditary
- 常染色体遗传
Medical Chinese dictionary (湘雅医学词典). 2013.
autosomal hereditary
Look at other dictionaries:
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
Hereditary hemorrhagic telangiectasia — Classification and external resources Characteristic lip telangiectases. ICD 10 I … Wikipedia
Hereditary nonpolyposis colorectal cancer — Classification and external resources ICD 10 C18 C20 ICD 9 … Wikipedia
Hereditary coproporphyria — Classification and external resources Coproporphyrinogen III ICD 10 E … Wikipedia
Hereditary mucoepithelial dysplasia — Classification and external resources ICD 10 L98.9 ICD 9 709.9 … Wikipedia
Hereditary equine regional dermal asthenia — (HERDA) aka hyperelastosis cutis (HC) is an inherited autosomal recessive connective tissue disorder. It develops from a homozygous recessive mutation that weakens collagen fibers that allow the skin of the animal to stay connected to the rest of … Wikipedia
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
Autosomal recessive distal spinal muscular atrophy 1 — Classification and external resources OMIM 604320 Autosomal recessive distal spinal muscular atrophy 1 (or spinal muscular atrophy with respiratory distress type 1, or distal spinal muscular atrophy 1)[1] … Wikipedia
Hereditary pyropoikilocytosis — (HPP) is an autosomal recessive form of hemolytic anemia characterized by an abnormal sensitivity of red blood cells to heat and erythrocyte morphology similar to that seen in thermal burns. Patients with HPP tend to experience severe haemolysis… … Wikipedia
Autosomal dominant hypophosphatemic rickets — (ADHR) is a rare hereditary disease in which excessive loss of phosphate in the urine leads to poorly formed bones (rickets), bone pain, and tooth abscesses. ADHR is caused by a mutation in the fibroblast growth factor 23 (FGF23). ADHR affects… … Wikipedia
