搜索结果
疾病ID:TCMBANKDI025794
疾病名:Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency
MeSH_Name:Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
HPO_Name:-
UMLS_Name:Disease or Syndrome
DO_Name:disease of metabolism; genetic disease
疾病类型:disease
DisGeNET_Link:C0268292
MeSH_Link:C16; C18; C13; C12; C19
HPO_Link:-
UMLS_Link:T047
DO_Link:DOID:0014667; DOID:630
HERB_ID:HBDIS006246
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 |
|---|
| TCMBANKGE000458 | CYP2B6 | CPB6; CYP2B; CYP2B7; CYP2B7P; CYPIIB6; EFVM; IIB1; P450 | cytochrome P450 family 2 subfamily B member 6 |
| TCMBANKGE000095 | CYP11B2 | ALDOS; CPN2; CYP11B; CYP11BL; CYPXIB2; P-450C18; P450C18; P450aldo | cytochrome P450 family 11 subfamily B member 2 |
| TCMBANKGE008796 | HSD17B6 | HSE; RODH; SDR9C6 | hydroxysteroid 17-beta dehydrogenase 6 |
| TCMBANKGE009297 | GML | LY6DL | glycosylphosphatidylinositol anchored molecule like |
| TCMBANKGE010121 | PPIG | CARS-Cyp; CYP; SCAF10; SRCyp | peptidylprolyl isomerase G |
| TCMBANKGE000471 | POMC | ACTH; CLIP; LPH; MSH; NPP; OBAIRH; POC | proopiomelanocortin |
| TCMBANKGE000941 | TXNRD1 | GRIM-12; TR; TR1; TRXR1; TXNR | thioredoxin reductase 1 |
| TCMBANKGE014262 | CYP11B1 | CPN1; CYP11B; FHI; P450C11 | cytochrome P450 family 11 subfamily B member 1 |
| TCMBANKGE006724 | REN | HNFJ2 | renin |
| TCMBANKGE004553 | CYP21A2 | CA21H; CAH1; CPS1; CYP21; CYP21B; P450c21B | cytochrome P450 family 21 subfamily A member 2 |
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Dai SX Lab