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疾病ID:TCMBANKDI006259
疾病名:Hereditary systemic amyloidosis
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:C4081731
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 |
|---|
| TCMBANKGE010980 | FGA | Fib2 | fibrinogen alpha chain |
| TCMBANKGE009389 | LYZ | LYZF1; LZM | lysozyme |
| TCMBANKGE001052 | NLRP3 | AGTAVPRL; AII; AVP; C1orf7; CIAS1; CLR1.1; DFNA34; FCAS; FCAS1; FCU; KEFH; MWS; NALP3; PYPAF1 | NLR family pyrin domain containing 3 |
| TCMBANKGE006656 | B2M | IMD43 | beta-2-microglobulin |
| TCMBANKGE005562 | USP9X | DFFRX; FAF; FAM; MRX99; MRXS99F | ubiquitin specific peptidase 9 X-linked |
| TCMBANKGE003921 | FANCF | FAF | FA complementation group F |
| TCMBANKGE005082 | APOA1 | HPALP2; apo(a) | apolipoprotein A1 |
| TCMBANKGE000934 | GFAP | ALXDRD | glial fibrillary acidic protein |
| TCMBANKGE011547 | APOC3 | APOCIII | apolipoprotein C3 |
| TCMBANKGE000643 | TTR | ATTR; CTS; CTS1; HEL111; HsT2651; PALB; TBPA | transthyretin |
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Dai SX Lab