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CCBE1

靶点ID:TCMBANKGE010892

靶点别名:HKLLS1

靶点描述:collagen and calcium binding EGF domains 1

染色体:18

染色体位置:18q21.32

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:29426

OMIM_Link:612753

Ensembl_Link:ENSG00000183287

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

TCMBANKDI000088	Neoplasms; Respiratory Tract Diseases	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	group
TCMBANKDI000166	-	-	Neoplastic Process	disease
TCMBANKDI002231	Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI002490	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI003385	Hemic and Lymphatic Diseases	Abnormality of the immune system; Abnormality of the respiratory system; Abnormality of the cardiovascular system	Finding	phenotype
TCMBANKDI003797	Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	group
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
TCMBANKDI006121	Digestive System Diseases; Neoplasms	Abnormality of the digestive system; Neoplasm	Neoplastic Process	group
TCMBANKDI006835	-	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI006900	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI007281	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI007610	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI008217	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI009422	-	-	Finding	phenotype
TCMBANKDI009572	Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Disease or Syndrome	phenotype
TCMBANKDI010203	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI013067	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI013675	Pathological Conditions, Signs and Symptoms	-	Organism Attribute	group
TCMBANKDI013728	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI013927	Respiratory Tract Diseases	Abnormality of the respiratory system	Pathologic Function	phenotype
TCMBANKDI014740	Pathological Conditions, Signs and Symptoms	Abnormality of the digestive system	Disease or Syndrome	phenotype
TCMBANKDI017024	Neoplasms; Respiratory Tract Diseases	-	Neoplastic Process	disease
TCMBANKDI018151	Digestive System Diseases; Nutritional and Metabolic Diseases	-	Disease or Syndrome	group
TCMBANKDI023060	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases	Abnormality of metabolism/homeostasis; Abnormality of prenatal development or birth	Disease or Syndrome	disease
TCMBANKDI025775	Hemic and Lymphatic Diseases	Abnormality of the immune system; Abnormality of the respiratory system; Abnormality of the cardiovascular system	Finding	phenotype
TCMBANKDI030664	Respiratory Tract Diseases	Abnormality of metabolism/homeostasis; Abnormality of the respiratory system	Disease or Syndrome	group
TCMBANKDI031802	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of head or neck; Abnormality of the skeletal system	Disease or Syndrome	disease