搜索结果
疾病ID:TCMBANKDI027131
疾病名:Peroxisome Biogenesis Disorder, Complementation Group C
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:C1832232
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 |
|---|
| TCMBANKGE001048 | TGM2 | TG(C); TGC | transglutaminase 2 |
| TCMBANKGE004092 | GGCT | C7orf24; CRF21; GCTG; GGC | gamma-glutamylcyclotransferase |
| TCMBANKGE000986 | ERBB2 | CD340; HER-2; HER-2/neu; HER2; MLN 19; NEU; NGL; TKR1 | erb-b2 receptor tyrosine kinase 2 |
| TCMBANKGE009233 | DNLZ | C9orf151; HEP; HEP1; TIMM15; ZIM17; bA413M3.2 | DNL-type zinc finger |
| TCMBANKGE004817 | SLC22A1 | HOCT1; OCT1; oct1_cds | solute carrier family 22 member 1 |
| TCMBANKGE006339 | CA2 | CA-II; CAC; CAII; Car2; HEL-76; HEL-S-282 | carbonic anhydrase 2 |
| TCMBANKGE000931 | CYP17A1 | CPT7; CYP17; P450C17; S17AH | cytochrome P450 family 17 subfamily A member 1 |
| TCMBANKGE006040 | SLC25A20 | CAC; CACT | solute carrier family 25 member 20 |
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Dai SX Lab