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疾病ID:TCMBANKDI019368


疾病名:Peroxisome Biogenesis Disorder, Complementation Group H


MeSH_Name:Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases


HPO_Name:-


UMLS_Name:Disease or Syndrome


DO_Name:disease of metabolism; genetic disease


疾病类型:disease


DisGeNET_Link:C1866260


MeSH_Link:C16; C18


HPO_Link:-


UMLS_Link:T047


DO_Link:DOID:0014667; DOID:630


HERB_ID:-


   疾病对应的植物
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

   疾病对应的化合物
化合物ID 化合物名 别名 分子式 分子质量 Smiles

   疾病对应的靶点
靶点ID 基因名 基因别名 描述
TCMBANKGE001033 FGFR1 BFGFR; CD331; CEK; ECCL; FGFBR; FGFR-1; FLG; FLT-2; FLT2; HBGFR; HH2; HRTFDS; KAL2; N-SAM; OGD; bFGF-R-1 fibroblast growth factor receptor 1
TCMBANKGE000986 ERBB2 CD340; HER-2; HER-2/neu; HER2; MLN 19; NEU; NGL; TKR1 erb-b2 receptor tyrosine kinase 2
TCMBANKGE000323 BRCA1 BRCAI; BRCC1; BROVCA1; FANCS; IRIS; PNCA4; PPP1R53; PSCP; RNF53 BRCA1 DNA repair associated
TCMBANKGE000932 AKT2 HIHGHH; PKBB; PKBBETA; PRKBB; RAC-BETA AKT serine/threonine kinase 2
TCMBANKGE001045 CCND1 BCL1; D11S287E; PRAD1; U21B31 cyclin D1