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IHH

靶点ID:TCMBANKGE000913

靶点别名:BDA1; HHG2

靶点描述:Indian hedgehog signaling molecule

染色体:2

染色体位置:2q35

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:5956

OMIM_Link:600726

Ensembl_Link:ENSG00000163501

靶点对应的植物

ID	拉丁名	药名	药用植物名	功能与主治	来源	药用部位	使用民族

靶点对应的化合物

化合物ID	化合物名	别名	分子式	分子质量	Smiles

TCMBANKIN060429	Cyclopamine		C27H41NO2	411.6 g/mol	CC1CC2C(C(C3(O2)CCC4C5CC=C6CC(CCC6(C5CC4=C3C)C)O)C)NC1

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000018	Digestive System Diseases; Neoplasms; Endocrine System Diseases	Abnormality of the digestive system; Neoplasm	Neoplastic Process	disease
TCMBANKDI000076	Neoplasms	-	Neoplastic Process	group
TCMBANKDI000166	-	-	Neoplastic Process	disease
TCMBANKDI000891	Neoplasms; Respiratory Tract Diseases	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	disease
TCMBANKDI001064	-	Growth abnormality	Finding	phenotype
TCMBANKDI001110	Neoplasms	Neoplasm	Neoplastic Process	disease
TCMBANKDI003353	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI003657	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI004802	Digestive System Diseases; Neoplasms	-	Neoplastic Process	disease
TCMBANKDI006121	Digestive System Diseases; Neoplasms	Abnormality of the digestive system; Neoplasm	Neoplastic Process	group
TCMBANKDI008217	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI009422	-	-	Finding	phenotype
TCMBANKDI011402	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI012416	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI013067	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI015420	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI015810	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI017642	Neoplasms	Abnormality of the integument; Neoplasm	Neoplastic Process	disease
TCMBANKDI017681	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of head or neck; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI019974	Skin and Connective Tissue Diseases	Abnormality of the integument	Finding	phenotype
TCMBANKDI023882	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI024262	-	-	Neoplastic Process	phenotype
TCMBANKDI025183	Digestive System Diseases	Abnormality of the digestive system; Abnormality of the nervous system	Pathologic Function	phenotype
TCMBANKDI025420	Digestive System Diseases; Neoplasms	Abnormality of the digestive system; Neoplasm	Neoplastic Process	disease
TCMBANKDI026573	Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI027752	-	Abnormality of the integument	Finding	phenotype
TCMBANKDI028305	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI028648	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI029220	Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI029922	Endocrine System Diseases	-	Disease or Syndrome	disease
TCMBANKDI030990	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI031498	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype