- familial ataxia
- Медицина: семейная атаксия
Универсальный англо-русский словарь. Академик.ру. 2011.
familial ataxia
Смотреть что такое "familial ataxia" в других словарях:
Friedreich familial ataxia — Friedreich familial ataxia. См. семейная атаксия Фридрейха. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) … Молекулярная биология и генетика. Толковый словарь.
Familial adenomatous polyposis — Classification and external resources Endoscopic image of sigmoid colon of patient with familial adenomatous polyposis. ICD 10 C … Wikipedia
Familial hemiplegic migraine — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 4693 ICD10 = ICD10|G|43|1|g|40 ICD9 = ICD9|346.8 ICDO = OMIM = 141500 OMIM mult = OMIM2|602481 OMIM2|609634 OMIM2|607516 MedlinePlus = eMedicineSubj = neuro eMedicineTopic = 219 Familial… … Wikipedia
Ataxia — For other uses, see Ataxia (disambiguation). Ataxia (from Greek α [used as a negative prefix] + τάξις [order], meaning lack of order ) is a neurological sign and symptom that consists of gross lack of coordination of muscle movements. Ataxia is a … Wikipedia
Ataxia telangiectasia — Infobox Disease Name = Ataxia Telangiectasia Caption = DiseasesDB = 1025 ICD10 = ICD10|G|11|3|g|10 ICD9 = ICD9|334.8 ICDO = OMIM = 208900 MedlinePlus = eMedicineSubj = derm eMedicineTopic = 691 eMedicine mult = eMedicine2|oph|319 MeshID = D001260 … Wikipedia
Familial isolated vitamin e deficiency — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 30633 ICD10 = ICD10|Group|Major|minor|LinkGroup|LinkMajor ICD9 = ICD9|xxx ICDO = OMIM = 277460 OMIM mult = OMIM2|600415 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Familial… … Wikipedia
Spinocerebellar ataxia type-6 — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 12339 ICD10 = ICD10|G|11|2|g|10 ICD9 = ICD9|334.9 ICDO = OMIM = 183086 MedlinePlus = eMedicineSubj = neuro eMedicineTopic = 556 Spinocerebellar ataxia type 6 (SCA6) is a rare, late onset,… … Wikipedia
Episodic ataxia — (EA) is an autosomal dominant disorder characterized by sporadic bouts of ataxia (severe discoordination) with or without myokymia (continuous muscle movement). Ataxia can be provoked by stress, startle, or heavy exertion such as exercise.… … Wikipedia
Friedreich's ataxia — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 4980 ICD10 = ICD10|G|11|1|g|10 ICD9 = ICD9|334.0 ICDO = OMIM = 229300 MedlinePlus = eMedicineSubj = neuro eMedicineTopic = 139 MeshID = D005621 Friedreich s ataxia is an inherited disease… … Wikipedia
Dunnigan familial partial lipodystrophy — Classification and external resources OMIM 151660 Dunnigan type familial partial lipodystrophy, abbreviated as (FPLD), is a rare monogenic form of insulin resistance characterized by loss of subcutaneous fat from the extremities, trunk, and… … Wikipedia
Multiple familial trichoepithelioma — (also known as Brooke–Spiegler syndrome and Epithelioma adenoides cysticum ) is a cutaneous condition characterized by multiple cystic and solid nodules appearing on the face.[1]:672 Types include: Type OMIM Gene Locus MFT1 601606 CYLD 16q12 q13… … Wikipedia
