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SHOX

靶点ID:TCMBANKGE004809

靶点别名:GCFX; PHOG; SHOXY; SS

靶点描述:short stature homeobox

染色体:X|Y

染色体位置:Xp22.33 and Yp11.2

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:10853

OMIM_Link:312865; 400020

Ensembl_Link:ENSG00000185960

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

TCMBANKDI001064	-	Growth abnormality	Finding	phenotype
TCMBANKDI003200	-	Abnormality of the musculature	Organ or Tissue Function	phenotype
TCMBANKDI003203	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI003261	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI003411	-	-	Disease or Syndrome	disease
TCMBANKDI003547	-	Abnormality of limbs; Abnormality of the skeletal system	Acquired Abnormality	disease
TCMBANKDI006326	Pathological Conditions, Signs and Symptoms	-	Congenital Abnormality	group
TCMBANKDI006900	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI007963	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI009422	-	-	Finding	phenotype
TCMBANKDI009731	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI011032	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI011402	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI011982	Nutritional and Metabolic Diseases; Musculoskeletal Diseases	Abnormality of the skeletal system	Disease or Syndrome	disease
TCMBANKDI012986	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI013169	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI013355	Musculoskeletal Diseases	-	Congenital Abnormality	disease
TCMBANKDI013407	Pathological Conditions, Signs and Symptoms	-	Disease or Syndrome	disease
TCMBANKDI013599	-	Growth abnormality	Disease or Syndrome	phenotype
TCMBANKDI017106	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases	Neoplasm; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI017577	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI017720	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI019825	Neoplasms	-	Neoplastic Process	disease
TCMBANKDI022065	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases	-	Disease or Syndrome	disease
TCMBANKDI022471	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases	-	Disease or Syndrome	disease
TCMBANKDI025070	-	-	Disease or Syndrome	disease
TCMBANKDI027401	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Congenital Abnormality	disease
TCMBANKDI028064	-	-	Disease or Syndrome	disease
TCMBANKDI028305	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI028400	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases	-	Disease or Syndrome	disease
TCMBANKDI031407	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI031498	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease