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HESX1

靶点ID:TCMBANKGE014368

靶点别名:ANF; CPHD5; RPX

靶点描述:HESX homeobox 1

染色体:3

染色体位置:3p14.3

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:4877

OMIM_Link:601802

Ensembl_Link:ENSG00000163666

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

TCMBANKDI000023	Skin and Connective Tissue Diseases; Immune System Diseases	Abnormality of the immune system	Disease or Syndrome	disease
TCMBANKDI001073	Cardiovascular Diseases	Abnormality of the cardiovascular system	Finding	phenotype
TCMBANKDI002456	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI003411	-	-	Disease or Syndrome	disease
TCMBANKDI003879	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI004086	Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Disease or Syndrome	disease
TCMBANKDI005226	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases	Abnormality of the nervous system; Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI005868	-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI006359	Endocrine System Diseases	Abnormality of the endocrine system; Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI007427	Eye Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI008387	Pathological Conditions, Signs and Symptoms	Abnormality of the genitourinary system; Abnormality of the endocrine system	Finding	phenotype
TCMBANKDI009870	-	Abnormality of the voice	Finding	disease
TCMBANKDI009935	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of the nervous system	Congenital Abnormality	disease
TCMBANKDI009951	Nutritional and Metabolic Diseases; Musculoskeletal Diseases	Abnormality of the skeletal system	Disease or Syndrome	disease
TCMBANKDI010589	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	disease
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI012420	Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	disease
TCMBANKDI015224	Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Respiratory Tract Diseases	Abnormality of the digestive system; Abnormality of the respiratory system	Anatomical Abnormality	disease
TCMBANKDI017308	Endocrine System Diseases	Abnormality of the endocrine system; Growth abnormality	Pathologic Function	phenotype
TCMBANKDI017469	Skin and Connective Tissue Diseases	Abnormality of the breast	Disease or Syndrome	disease
TCMBANKDI018929	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI019267	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Sign or Symptom	phenotype
TCMBANKDI019973	Endocrine System Diseases	-	Disease or Syndrome	disease
TCMBANKDI020860	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases	Abnormality of the digestive system	Congenital Abnormality	disease
TCMBANKDI021151	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI021525	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Endocrine System Diseases	-	Disease or Syndrome	disease
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024559	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI027319	Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI027961	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	Abnormality of the nervous system	Congenital Abnormality	disease
TCMBANKDI029321	Cardiovascular Diseases	-	Disease or Syndrome	group
TCMBANKDI029922	Endocrine System Diseases	-	Disease or Syndrome	disease
TCMBANKDI030411	Digestive System Diseases	Abnormality of the digestive system	Finding	phenotype
TCMBANKDI031417	Skin and Connective Tissue Diseases	Abnormality of the integument	Sign or Symptom	phenotype
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI032109	Pathological Conditions, Signs and Symptoms	-	Disease or Syndrome	disease