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NEB

靶点ID:TCMBANKGE009953

靶点别名:NEB177D; NEM2

靶点描述:nebulin

染色体:2

染色体位置:2q23.3

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:7720

OMIM_Link:161650

Ensembl_Link:ENSG00000183091

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

TCMBANKDI000121	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system; Abnormality of the musculature	Finding	phenotype
TCMBANKDI000891	Neoplasms; Respiratory Tract Diseases	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	disease
TCMBANKDI002840	Musculoskeletal Diseases; Nervous System Diseases	-	Disease or Syndrome; Congenital Abnormality	disease
TCMBANKDI003685	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of prenatal development or birth	Disease or Syndrome	disease
TCMBANKDI004222	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI004489	-	Abnormality of the ear	Congenital Abnormality	disease
TCMBANKDI006028	-	Abnormality of the musculature	Finding	phenotype
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
TCMBANKDI007343	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	-	Finding	phenotype
TCMBANKDI007770	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype
TCMBANKDI007856	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI008874	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI009106	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases	-	Disease or Syndrome	disease
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI012319	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI013913	Nervous System Diseases	Abnormality of the musculature	Sign or Symptom	phenotype
TCMBANKDI013927	Respiratory Tract Diseases	Abnormality of the respiratory system	Pathologic Function	phenotype
TCMBANKDI013994	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI015863	-	Abnormality of the nervous system; Abnormality of the musculature	Finding	phenotype
TCMBANKDI016031	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI016179	-	Abnormality of metabolism/homeostasis; Abnormal cellular phenotype	Finding	phenotype
TCMBANKDI017869	Nervous System Diseases	Abnormality of the nervous system; Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI018761	-	-	Diagnostic Procedure	phenotype
TCMBANKDI018929	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI018939	Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI019650	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	-	Disease or Syndrome	phenotype
TCMBANKDI020119	Mental Disorders	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI020334	Musculoskeletal Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI020373	-	Abnormality of the musculature	Pathologic Function	phenotype
TCMBANKDI020574	Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Stomatognathic Diseases	Abnormality of the nervous system; Abnormality of head or neck; Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI020942	-	-	Laboratory Procedure	phenotype
TCMBANKDI021038	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI021233	Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Stomatognathic Diseases	Abnormality of the nervous system; Abnormality of head or neck; Abnormality of the musculature	Sign or Symptom	phenotype
TCMBANKDI022380	Female Urogenital Diseases and Pregnancy Complications	Abnormality of prenatal development or birth	Pathologic Function	phenotype
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
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024199	-	Abnormality of limbs; Abnormality of the skeletal system; Abnormality of the musculature	Finding	phenotype
TCMBANKDI027248	Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI027406	-	Abnormality of the nervous system; Abnormality of the musculature	Finding	phenotype
TCMBANKDI027657	-	Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI027721	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system; Abnormality of connective tissue; Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI031447	-	Abnormality of the musculature	Finding	phenotype
TCMBANKDI031753	-	Abnormality of the musculature	Finding	phenotype
TCMBANKDI032109	Pathological Conditions, Signs and Symptoms	-	Disease or Syndrome	disease