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BBS5

靶点ID:TCMBANKGE010082

靶点别名:-

靶点描述:Bardet-Biedl syndrome 5

染色体:2

染色体位置:2q31.1

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:970

OMIM_Link:603650

Ensembl_Link:ENSG00000163093

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

TCMBANKDI002718		-	-	Finding	phenotype
TCMBANKDI002881		-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI003879		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI005587		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI007228		-	-	Finding	phenotype
TCMBANKDI008314		Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI015186		-	Abnormality of the nervous system	Anatomical Abnormality	phenotype
TCMBANKDI020373		-	Abnormality of the musculature	Pathologic Function	phenotype
TCMBANKDI020842		-	-	Finding	phenotype
TCMBANKDI021924		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases	-	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
TCMBANKDI028799		Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI032191		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases	-	Disease or Syndrome	disease