搜索结果
疾病ID:TCMBANKDI005876
疾病名:WAARDENBURG SYNDROME, TYPE IIA
MeSH_Name:Congenital, Hereditary, and Neonatal Diseases and Abnormalities
HPO_Name:-
UMLS_Name:Disease or Syndrome
DO_Name:genetic disease
疾病类型:disease
DisGeNET_Link:C1860339
MeSH_Link:C16
HPO_Link:-
UMLS_Link:T047
DO_Link: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 |
|---|
| TCMBANKGE008559 | GJB2 | BAPS; CX26; DFNA3; DFNA3A; DFNB1; DFNB1A; HID; KID; NSRD1; PPK | gap junction protein beta 2 |
| TCMBANKGE003676 | POLR2F | HRBP14.4; POLRF; RPABC14.4; RPABC2; RPB14.4; RPB6; RPC15 | RNA polymerase II, I and III subunit F |
| TCMBANKGE007797 | KITLG | DCUA; DFNA69; FPH2; FPHH; KL-1; Kitl; MGF; SCF; SF; SHEP7; SLF | KIT ligand |
| TCMBANKGE000377 | MITF | CMM8; COMMAD; MI; WS2; WS2A; bHLHe32 | melanocyte inducing transcription factor |
| TCMBANKGE005857 | Pax3 | Pax-3; Sp; Splchl2; splotch | paired box 3 |
滇IICP备16009434号-1 |
Dai SX Lab