YEM Search

搜索结果

LMX1B

靶点ID:TCMBANKGE012181

靶点别名:LMX1.2; NPS1

靶点描述:LIM homeobox transcription factor 1 beta

染色体:9

染色体位置:9q33.3

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:6654

OMIM_Link:602575

Ensembl_Link:ENSG00000136944

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

TCMBANKDI000061	Digestive System Diseases; Neoplasms	Abnormality of the digestive system; Neoplasm	Neoplastic Process	group
TCMBANKDI000066	Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI001299	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI001877	-	Abnormality of limbs; Abnormality of the musculature	Finding	phenotype
TCMBANKDI002278	Nervous System Diseases; Mental Disorders	-	Disease or Syndrome	disease
TCMBANKDI003261	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI003353	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI003547	-	Abnormality of limbs; Abnormality of the skeletal system	Acquired Abnormality	disease
TCMBANKDI007281	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI007362	Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases	-	Disease or Syndrome	disease
TCMBANKDI007520	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI007994	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI008206	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Congenital Abnormality	group
TCMBANKDI008314	Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI008354	-	Abnormality of limbs; Abnormality of the musculature	Finding	phenotype
TCMBANKDI013067	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI013453	Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system	Finding	phenotype
TCMBANKDI013784	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI015485	Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI016330	Mental Disorders	-	Mental or Behavioral Dysfunction	disease
TCMBANKDI016890	Digestive System Diseases; Neoplasms	-	Neoplastic Process	disease
TCMBANKDI018929	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI020297	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI022485	-	-	Diagnostic Procedure	phenotype
TCMBANKDI024870	Pathological Conditions, Signs and Symptoms	Abnormality of the integument	Congenital Abnormality	disease
TCMBANKDI027581	Nervous System Diseases; Mental Disorders	-	Sign or Symptom	phenotype
TCMBANKDI029054	Mental Disorders	-	Mental or Behavioral Dysfunction	group
TCMBANKDI029783	-	-	Diagnostic Procedure	phenotype
TCMBANKDI029818	Nervous System Diseases; Mental Disorders	-	Disease or Syndrome	disease
TCMBANKDI030540	Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases	Abnormality of the genitourinary system; Neoplasm	Neoplastic Process	disease
TCMBANKDI031258	Nervous System Diseases; Mental Disorders	-	Disease or Syndrome	disease
TCMBANKDI032109	Pathological Conditions, Signs and Symptoms	-	Disease or Syndrome	disease
TCMBANKDI032350	Pathological Conditions, Signs and Symptoms; Eye Diseases; Skin and Connective Tissue Diseases	Abnormality of the eye	Finding	phenotype
TCMBANKDI032496	Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Disease or Syndrome	disease