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疾病ID:TCMBANKDI006486
疾病名:Heredodegenerative Disorders, Nervous System
MeSH_Name:Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
HPO_Name:-
UMLS_Name:Disease or Syndrome
DO_Name:-
疾病类型:group
DisGeNET_Link:C0751870
MeSH_Link:C16; C10
HPO_Link:-
UMLS_Link:T047
DO_Link:-
HERB_ID:HBDIS011492
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 |
|---|
| TCMBANKGE001089 | PARP1 | ADPRT; ADPRT 1; ADPRT1; ARTD1; PARP; PARP-1; PPOL; pADPRT-1 | poly(ADP-ribose) polymerase 1 |
| TCMBANKGE000526 | ATXN1 | ATX1; D6S504E; SCA1 | ataxin 1 |
| TCMBANKGE012856 | ATXN3 | AT3; ATX3; JOS; MJD; MJD1; SCA3 | ataxin 3 |
| TCMBANKGE000364 | SMN1 | BCD541; GEMIN1; SMA; SMA1; SMA2; SMA3; SMA4; SMA@; SMN; SMNT; T-BCD541; TDRD16A | survival of motor neuron 1, telomeric |
| TCMBANKGE002022 | XRCC1 | RCC; SCAR26 | X-ray repair cross complementing 1 |
| TCMBANKGE011387 | CYGB | HGB; STAP | cytoglobin |
| TCMBANKGE000951 | CYP7B1 | CBAS3; CP7B; SPG5A | cytochrome P450 family 7 subfamily B member 1 |
| TCMBANKGE005810 | HTT | HD; IT15; LOMARS | huntingtin |
| TCMBANKGE006834 | FTL | LFTD; NBIA3 | ferritin light chain |
| TCMBANKGE000643 | TTR | ATTR; CTS; CTS1; HEL111; HsT2651; PALB; TBPA | transthyretin |
| TCMBANKGE007230 | FXN | CyaY; FA; FARR; FRDA; X25 | frataxin |
| TCMBANKGE001200 | STMN1 | C1orf215; LAP18; Lag; OP18; PP17; PP19; PR22; SMN | stathmin 1 |
| TCMBANKGE011207 | NGB | - | neuroglobin |
| TCMBANKGE010583 | SMN2 | BCD541; C-BCD541; GEMIN1; SMNC; TDRD16B | survival of motor neuron 2, centromeric |
| TCMBANKGE012046 | ARSA | ASA; MLD | arylsulfatase A |
| TCMBANKGE001071 | NPC1 | NPC; POGZ; SLC65A1 | NPC intracellular cholesterol transporter 1 |
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