a group of rare disorders in which too many langerhans cells (a type of white blood cell) grow in certain tissues and organs including the bones, skin, and lungs, and damage them. lch may also affect the pituitary gland (which makes hormones that control other glands and many body functions, especially growth). lch is most common in children and young adults. also called langerhans cell histiocytosis.
fly | 遺伝子名 | LCH |
同義語(エイリアス) | 2LCH; l(3)00035; CG1469; Ferritin 2 light chain homologue; Ferritin; Ferritin-Heavy; Fer-H: Ferritin-Heavy; anon-EST:ParkEST264; Fer2LCH; l(3)j2A3; l(3)neo63; l(3)07016; l(3)s2083; l(3)neo60 | |
SWISS-PROTのID | --- | |
EntrezGeneのID | EntrezGene:44965 | |
その他のDBのID | FlyBase:FBgn0015221 |
human | 遺伝子名 | LCH |
同義語(エイリアス) | Lentil agglutinin-binding | |
SWISS-PROTのID | --- | |
EntrezGeneのID | EntrezGene:8118 |
mouse | 遺伝子名 | Lch |
同義語(エイリアス) | low cholesterol; low HDL cholesterol | |
SWISS-PROTのID | --- | |
EntrezGeneのID | EntrezGene:117562 | |
その他のDBのID | MGI:2152768 |
本文中に表示されているデータベースの説明