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疾病ID:TCMBANKDI004967
疾病名:Carnitine palmitoyl transferase 2 deficiency
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:C0342790
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 |
|---|
| TCMBANKGE013324 | GBE1 | APBD; GBE; GSD4 | 1,4-alpha-glucan branching enzyme 1 |
| TCMBANKGE000165 | ETFDH | ETFQO; MADD | electron transfer flavoprotein dehydrogenase |
| TCMBANKGE010756 | CPT2 | CPT1; CPTASE; IIAE4 | carnitine palmitoyltransferase 2 |
| TCMBANKGE001105 | CS | - | citrate synthase |
| TCMBANKGE007911 | HADHA | ECHA; GBP; HADH; LCEH; LCHAD; MTPA; TP-ALPHA | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha |
| TCMBANKGE001140 | FGF21 | - | fibroblast growth factor 21 |
| TCMBANKGE006040 | SLC25A20 | CAC; CACT | solute carrier family 25 member 20 |
| TCMBANKGE013791 | DHDDS | CIT; CPT; DEDSM; DS; HDS; RP59; hCIT | dehydrodolichyl diphosphate synthase subunit |
| TCMBANKGE010522 | EHHADH | ECHD; FRTS3; L-PBE; LBFP; LBP; PBFE | enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase |
| TCMBANKGE000021 | MB | PVALB | myoglobin |
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