OMIM → Related disease, drugs, ...
Query OMIM entry list
01
608776
CDG1L
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il
-
Disease
:
Chemicals
:
Biological Phenomena
:
Anatomy
:
Organisms
Disease
→
Tree View
MeSH term
Japanese
Link
01
Congenital Disorders of Glycosylation
先天性グリコシル化異常症
Hepatomegaly
肝腫脹
Muscle Hypotonia
筋緊張低下
Seizures
けいれん性発作
Chemicals
→
Tree View
MeSH term
Japanese
Link
01
Mannosyltransferases
マンノシルトランスフェラーゼ
Saccharomyces cerevisiae Proteins
サッカロミセスセレビシエ蛋白質
Lipopolysaccharides
リポ多糖類
Biological Phenomena
→
Tree View
MeSH term
Japanese
Link
01
Glycosylation
-
Amino Acid Substitution
アミノ酸置換
Sequence Homology, Amino Acid
アミノ酸配列相同性
Homozygote
ホモ接合体
Point Mutation
点変異
Amino Acid Sequence
アミノ酸配列
Anatomy
→
Tree View
MeSH term
Japanese
Link
01
Organisms
→
Tree View
MeSH term
Japanese
Link
01
Saccharomyces cerevisiae
酵母-パン
Humans
ヒト
Database Center for Life Science