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疾病ID:TCMBANKDI003177
疾病名:Jervell-Lange Nielsen Syndrome
MeSH_Name:Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
HPO_Name:-
UMLS_Name:Disease or Syndrome
DO_Name:disease of anatomical entity
疾病类型:disease
DisGeNET_Link:C0022387
MeSH_Link:C16; C14
HPO_Link:-
UMLS_Link:T047
DO_Link:DOID:7
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 |
|---|
| TCMBANKGE002442 | NT5E | CALJA; CD73; E5NT; NT; NT5; NTE; eN; eNT | 5'-nucleotidase ecto |
| TCMBANKGE000121 | KCNH2 | ERG-1; ERG1; H-ERG; HERG; HERG1; Kv11.1; LQT2; SQT1 | potassium voltage-gated channel subfamily H member 2 |
| TCMBANKGE003231 | KCNE1 | ISK; JLNS; JLNS2; LQT2/5; LQT5; MinK | potassium voltage-gated channel subfamily E regulatory subunit 1 |
| TCMBANKGE000574 | GAST | GAS | gastrin |
| TCMBANKGE008327 | KCNQ4 | DFNA2; DFNA2A; KV7.4 | potassium voltage-gated channel subfamily Q member 4 |
| TCMBANKGE000889 | HFE | HFE1; HH; HLA-H; MVCD7; TFQTL2 | homeostatic iron regulator |
| TCMBANKGE000309 | SCN5A | CDCD2; CMD1E; CMPD2; HB1; HB2; HBBD; HH1; ICCD; IVF; LQT3; Nav1.5; PFHB1; SSS1; VF1 | sodium voltage-gated channel alpha subunit 5 |
| TCMBANKGE000302 | KCNQ1 | ATFB1; ATFB3; JLNS1; KCNA8; KCNA9; KVLQT1; Kv1.9; Kv7.1; LQT; LQT1; RWS; SQT2; WRS | potassium voltage-gated channel subfamily Q member 1 |
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Dai SX Lab