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BBS10

靶点ID:TCMBANKGE007247

靶点别名:C12orf58

靶点描述:Bardet-Biedl syndrome 10

染色体:12

染色体位置:12q21.2

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:26291

OMIM_Link:610148

Ensembl_Link:ENSG00000179941

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

TCMBANKIN031363	dimethyl sulfoxide		C2H6OS	78.14 g/mol	CS(=O)C

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI002718		-	-	Finding	phenotype
TCMBANKDI002742		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	group
TCMBANKDI002881		-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI003248		Nutritional and Metabolic Diseases; Endocrine System Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease
TCMBANKDI003657		-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI003879		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI007228		-	-	Finding	phenotype
TCMBANKDI007314		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI007957		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases	Abnormality of the ear	Disease or Syndrome	disease
TCMBANKDI014753		-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI020373		-	Abnormality of the musculature	Pathologic Function	phenotype
TCMBANKDI023751		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI025183		Digestive System Diseases	Abnormality of the digestive system; Abnormality of the nervous system	Pathologic Function	phenotype
TCMBANKDI030734		-	-	Finding	disease
TCMBANKDI032191		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases	-	Disease or Syndrome	disease