OMIM → Related disease, drugs, ...

Query OMIM entry list

01	228900	-	FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY	-

Disease

→ Tree View

	MeSH term	Japanese	Link	01
	Foot Deformities, Congenital	足の形態異常-先天性
	Hand Deformities, Congenital	手の形態異常-先天性
	Limb Deformities, Congenital	四肢奇形-先天性
	Dwarfism	低身長症
	Syndrome	症候群

---

Chemicals

→ Tree View

	MeSH term	Japanese	Link	01
	Bone Morphogenetic Proteins	骨形成因子

---

Biological Phenomena

→ Tree View

	MeSH term	Japanese	Link	01
	Genes, Recessive	劣性遺伝子
	Consanguinity	血族
	Mutation, Missense	ミスセンス変異
	Homozygote	ホモ接合体
	Point Mutation	点変異
	Phenotype	表現型

---

Anatomy

→ Tree View

	MeSH term	Japanese	Link	01
	Fibula	腓骨
	Toes	足指
	Fingers	手指

---

Organisms

→ Tree View

	MeSH term	Japanese	Link	01
	Humans	ヒト

---

Database Center for Life Science