OMIM → Related disease, drugs, ...
Query OMIM entry list
01
608779
CDG2E
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe
-
Disease
:
Chemicals
:
Biological Phenomena
:
Anatomy
:
Organisms
Disease
→
Tree View
MeSH term
Japanese
Link
01
Carbohydrate Metabolism, Inborn Errors
炭水化物代謝異常-先天性
Chemicals
→
Tree View
MeSH term
Japanese
Link
01
DNA, Complementary
相補的DNA
Carrier Proteins
担体蛋白質
Biological Phenomena
→
Tree View
MeSH term
Japanese
Link
01
Glycosylation
-
Homozygote
ホモ接合体
Base Sequence
塩基配列
Mutation
変異
Anatomy
→
Tree View
MeSH term
Japanese
Link
01
Golgi Apparatus
Golgi装置
Organisms
→
Tree View
MeSH term
Japanese
Link
01
Humans
ヒト
Database Center for Life Science