搜索结果
疾病ID:TCMBANKDI029633
疾病名:Carnitine-Acylcarnitine Translocase Deficiency
MeSH_Name:Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
HPO_Name:-
UMLS_Name:Disease or Syndrome
DO_Name:-
疾病类型:disease
DisGeNET_Link:C0342791
MeSH_Link:C16; C18
HPO_Link:-
UMLS_Link:T047
DO_Link:-
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 |
|---|
| TCMBANKGE014422 | SLC16A1 | HHF7; MCT; MCT1; MCT1D | solute carrier family 16 member 1 |
| TCMBANKGE014881 | MCAT | FASN2C; MCT; MCT1; MT; NET62; fabD | malonyl-CoA-acyl carrier protein transacylase |
| TCMBANKGE008899 | IDS | ID2S; MPS2; SIDS | iduronate 2-sulfatase |
| TCMBANKGE007911 | HADHA | ECHA; GBP; HADH; LCEH; LCHAD; MTPA; TP-ALPHA | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha |
| TCMBANKGE003819 | MCPH1 | BRIT1; MCT | microcephalin 1 |
| TCMBANKGE006040 | SLC25A20 | CAC; CACT | solute carrier family 25 member 20 |
| TCMBANKGE000475 | NCOA3 | ACTR; AIB-1; AIB1; CAGH16; CTG26; KAT13B; RAC3; SRC-3; SRC3; TNRC14; TNRC16; TRAM-1; bHLHe42; pCIP | nuclear receptor coactivator 3 |
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Dai SX Lab