OMIM → Related disease, drugs, ...

Query OMIM entry list

01	212720	-	MARTSOLF SYNDROME	-

Disease

→ Tree View

	MeSH term	Japanese	Link	01
	Cataract	白内障
	Intellectual Disability	精神発達遅滞
	Abnormalities, Multiple	奇形-多発
	Syndrome	症候群
	Hypogonadism	性機能低下症
	Microcephaly	小頭症
	Growth Disorders	成長障害
	Cockayne Syndrome	Cockayne症候群
	Cryptorchidism	停留精巣
	Xeroderma Pigmentosum	乾皮症-色素性
	Fetal Diseases	胎児疾患
	Bone Diseases, Developmental	骨発育異常
	Osteoporosis	骨粗鬆症
	Dwarfism	低身長症
	Atrophy	萎縮

---

Chemicals

→ Tree View

	MeSH term	Japanese	Link	01
	rab3 GTP-Binding Proteins	rab3 GTP結合蛋白質
	Xeroderma Pigmentosum Group D Protein	-
	DNA Helicases	DNAヘリカーゼ
	Transcription Factors	転写因子
	DNA-Binding Proteins	DNA結合タンパク
	Proteins	蛋白質

---

Biological Phenomena

→ Tree View

	MeSH term	Japanese	Link	01
	Body Height	身長
	Triplets	三胎
	Mutation, Missense	ミスセンス変異
	Catalytic Domain	触媒ドメイン
	Base Pair Mismatch	ミスマッチ塩基対
	DNA Replication	DNA複製
	Ultraviolet Rays	紫外線
	RNA Splicing	RNAスプライシング
	DNA Repair	DNA修復
	Pregnancy	妊娠
	Amino Acid Sequence	アミノ酸配列
	Base Sequence	塩基配列

---

Anatomy

→ Tree View

	MeSH term	Japanese	Link	01
	Cerebellum	小脳
	Joints	関節
	Cerebral Cortex	大脳皮質
	Face	顔面

---

Organisms

→ Tree View

	MeSH term	Japanese	Link	01
	Humans	ヒト

---

Database Center for Life Science