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ARVCF

靶点ID:TCMBANKGE006929

靶点别名:-

靶点描述:ARVCF delta catenin family member

染色体:22

染色体位置:22q11.21

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:728

OMIM_Link:602269

Ensembl_Link:ENSG00000099889

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

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000054	Nervous System Diseases; Mental Disorders	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI000066	Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI001779	Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI002742	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	group
TCMBANKDI002881	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI003879	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI004489	-	Abnormality of the ear	Congenital Abnormality	disease
TCMBANKDI004646	Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI005528	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	-	Congenital Abnormality	disease
TCMBANKDI006900	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI007031	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI007110	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI007281	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI007314	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI007610	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI007618	Hemic and Lymphatic Diseases	Abnormality of blood and blood-forming tissues	Disease or Syndrome	phenotype
TCMBANKDI007856	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI008874	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI009572	Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Disease or Syndrome	phenotype
TCMBANKDI010792	Mental Disorders	-	Mental or Behavioral Dysfunction	disease
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI011776	Digestive System Diseases	Abnormality of the digestive system; Constitutional symptom	Disease or Syndrome	disease
TCMBANKDI011883	-	-	Mental Process	phenotype
TCMBANKDI012319	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI013067	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI013730	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	Abnormality of the cardiovascular system	Congenital Abnormality	disease
TCMBANKDI014645	Pathological Conditions, Signs and Symptoms	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI015460	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Respiratory Tract Diseases; Otorhinolaryngologic Diseases	Abnormality of the respiratory system	Congenital Abnormality	disease
TCMBANKDI015485	Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI016700	Mental Disorders	-	Mental or Behavioral Dysfunction	disease
TCMBANKDI017673	-	-	Clinical Attribute	phenotype
TCMBANKDI018929	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI019546	-	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI022380	Female Urogenital Diseases and Pregnancy Complications	Abnormality of prenatal development or birth	Pathologic Function	phenotype
TCMBANKDI022394	-	-	Laboratory Procedure	phenotype
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI025171	Otorhinolaryngologic Diseases	Abnormality of the immune system; Abnormality of the ear	Disease or Syndrome	disease
TCMBANKDI025221	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of head or neck; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI025632	Mental Disorders	-	Mental or Behavioral Dysfunction	disease
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI032109	Pathological Conditions, Signs and Symptoms	-	Disease or Syndrome	disease