- variable penetrance
- Общая лексика: при переменной пенетрантности (если в тексте оригинала употребляется с предлогом with)
Универсальный англо-русский словарь. Академик.ру. 2011.
Универсальный англо-русский словарь. Академик.ру. 2011.
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
Lethal white syndrome — (LWS), also called overo lethal white syndrome (OLWS), lethal white overo (LWO), and overo lethal white foal syndrome (OLWFS), is an autosomal genetic disorder most prevalent in the American Paint Horse. Affected foals are born after the full 11… … Wikipedia
Hereditary elliptocytosis — Classification and external resources Blood smear showing elliptocytes ICD 10 D … Wikipedia
Holoprosencephaly — A disorder characterized by the failure of the prosencephalon (the forebrain of the embryo) to develop. During normal development, the forebrain is formed and the face begins to develop in the fifth and sixth weeks of pregnancy. Holoprosencephaly … Medical dictionary
Restless legs syndrome — Infobox Disease Name = Restless legs syndrome Caption = Sleep pattern of a Restless Legs Syndrome patient (red) vs. a healthy sleep pattern (blue). DiseasesDB = 29476 ICD10 = ICD10|G|25|8|g|20 ICD9 = ICD9|333.94 ICDO = OMIM = 102300 OMIM mult =… … Wikipedia
Chronic pancreatitis — Classification and external resources ICD 10 K86.0 K86.1 ICD 9 … Wikipedia
Cleft chin — Example of a cleft chin (William McKinley) Human jaw front view … Wikipedia
Progressive retinal atrophy — (PRA) is a group of genetic diseases seen in certain breeds of dogs and, more rarely, cats. It is characterized by the bilateral degeneration of the retina, causing progressive vision loss culminating in blindness. The condition in nearly all… … Wikipedia
Infantile cortical hyperostosis — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 29307 ICD10 = ICD10|M|89|8|m|86 ICD9 = ICD9|756.59 ICDO = OMIM = 114000 MedlinePlus = eMedicineSubj = orthoped eMedicineTopic = 151 MeshID = D006958 Infantile cortical hyperostosis is a self… … Wikipedia
Leopard syndrome — Infobox Disease Name = LEOPARD syndrome Caption = DiseasesDB = 7387 ICD10 = ICD9 = ICDO = OMIM = 151100 MedlinePlus = eMedicineSubj = derm eMedicineTopic = 627 MeshName = LEOPARD+Syndrome MeshNumber = C05.660.207.525 LEOPARD syndrome is a rare… … Wikipedia
CHRNE — Cholinergic receptor, nicotinic, epsilon, also known as CHRNE, is a human gene.cite web | title = Entrez Gene: CHRNE cholinergic receptor, nicotinic, epsilon| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… … Wikipedia