Мы используем Cookies Этот веб-сайт использует cookie-файлы, чтобы предлагать вам наиболее актуальную информацию. Просматривая этот веб-сайт, Вы принимаете cookie-файлы.
Знаете ли вы? Кликните два раза на слово, чтобы найти его в TermGallery.
Значения термина recessive disorder на английском
Значения для термина "recessive disorder" отсутствуют.
Использование термина recessive disorder на английском
1
Fucosidosis is a rare autosomal recessivedisorder resulting from a deficiency of alpha-L-fucosidase.
2
This autosomal recessivedisorder is present in members of three consanguineous Saudi Arabian families.
3
We report a family with an X-linked recessivedisorder characterized by muscle cramps and myalgia.
4
Purpose: Lowe syndrome is a rare, X-linked recessivedisorder caused by mutations in the OCRL gene.
5
Perrault syndrome is a genetically heterogeneous recessivedisorder characterized by ovarian dysgenesis and sensorineural hearing loss.
6
Background: The recessivedisorder trimethylaminuria is caused by defects in the FMO3 gene, and may be associated with hypertension.
7
Congenital afibrinogenemia is a rare autosomal recessivedisorder associated with an increased risk of hemorrhage, thrombosis, and obstetric complications.
8
Shwachman-Diamond syndrome (SDS) is a recessivedisorder typified by bone marrow failure and predisposition to hematological malignancies.
9
Purpose: Wilson disease, an autosomal recessivedisorder of copper transport, is probably the most common inherited metabolic disorder in Korea.
10
Congenital atransferrinemia is an extremely rare autosomal recessivedisorder resulting in the complete absence or extremely reduced amount of transferrin.
11
Wilson's disease is an autosomal recessivedisorder of copper transport caused by mutations in the gene encoding an ATPase, ATP7B.
12
In humans, sulfite oxidase deficiency is an inherited recessivedisorder that produces severe neonatal neurological problems that lead to early death.
13
Adrenoleukodystrophy (ALD) is an X-linked recessivedisorder that affects mainly the nervous system white matter and the adrenal cortex.
14
Childhood proximal spinal muscular atrophy (SMA) is an autosomal recessivedisorder which presents as a severe, intermediate or mild condition.
15
Menkes disease is a severe X-linked recessivedisorder caused by a defect in the ATP7A gene, which encodes a membrane copper-transporting ATPase.
16
PC deficiency is a rare autosomal recessivedisorder with three clinical presentations: an infantile form, a severe neonatal form, and a benign form.