- hereditary defect
- наследственный дефект
English-russian dctionary of contemporary Economics. 2014.
hereditary defect
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Hereditary nonpolyposis colorectal cancer — Classification and external resources ICD 10 C18 C20 ICD 9 … Wikipedia
Hereditary elliptocytosis — Classification and external resources Blood smear showing elliptocytes ICD 10 D … 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
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
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
Hereditary spherocytosis (HS) — A genetic disorder of the red blood cell membrane clinically characterized by anemia, jaundice (yellowing) and splenomegaly (enlargement of the spleen). In HS the red cells are smaller, rounder, and more fragile than normal. The red cells have a… … Medical dictionary
defect — Synonyms and related words: abandon, abnormality, acute disease, affection, affliction, ailment, allergic disease, allergy, apostacize, apostatize, arrearage, atrophy, back out, bacterial disease, betray, birth defect, birthmark, blackhead, bleb … Moby Thesaurus
Leber's hereditary optic neuropathy — Classification and external resources ICD 10 H47.2 ICD 9 377.16 … Wikipedia
Thyroid hormone organification defect IIb — This condition, clinically called Pendred syndrome, is the hereditary association of congenital deafness (deafness at the time of birth) and goiter (enlargement of the thyroid gland in the front of the neck) due to a defect in the making of… … Medical dictionary
autosomal recessive defect — noun a disease caused by the presence of two recessive mutant genes on an autosome • Syn: ↑autosomal recessive disease • Hypernyms: ↑genetic disease, ↑genetic disorder, ↑genetic abnormality, ↑genetic defect, ↑congenital … Useful english dictionary
