human | 遺伝子名 | erythrokeratodermia variabilis |
同義語(エイリアス) | ||
SWISS-PROTのID | --- | |
EntrezGeneのID | --- | |
その他のDBのID | HGNC:3307 |
本文中に表示されているデータベースの説明
出典:Wiktionary
出典:Wikipedia
出典:『Wikipedia』 (2010/12/17 03:57 UTC 版)
Erythrokeratodermia variabilis (also known as "Erythrokeratodermia figurata variabilis," "Keratosis extremitatum progrediens," "Keratosis palmoplantaris transgrediens et progrediens,":509 "Mendes da Costa syndrome," "Mendes da Costa type erythrokeratodermia," and "Progressive symmetric erythrokeratoderma") is a rare autosomal dominant disorder that usually presents at birth or during the first year of life.