搜索结果
疾病ID:TCMBANKDI025265
疾病名:ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA
MeSH_Name:Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
HPO_Name:-
UMLS_Name:Disease or Syndrome
DO_Name:disease of anatomical entity
疾病类型:disease
DisGeNET_Link:C0220666
MeSH_Link:C16; C05; C07
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 |
|---|
| TCMBANKGE002324 | KCNJ1 | KIR1.1; ROMK; ROMK1 | potassium inwardly rectifying channel subfamily J member 1 |
| TCMBANKGE003571 | ECEL1 | DA5D; DINE; ECEX; XCE | endothelin converting enzyme like 1 |
| TCMBANKGE004283 | FBN2 | CCA; DA9; EOMD | fibrillin 2 |
| TCMBANKGE004879 | WNK1 | HSAN2; HSN2; KDP; PPP1R167; PRKWNK1; PSK; p65 | WNK lysine deficient protein kinase 1 |
| TCMBANKGE005283 | CUL3 | CUL-3; PHA2E | cullin 3 |
| TCMBANKGE000356 | SLC12A2 | BSC; BSC2; NKCC1; PPP1R141 | solute carrier family 12 member 2 |
| TCMBANKGE014567 | SLC12A3 | NCC; NCCT; TSC | solute carrier family 12 member 3 |
| TCMBANKGE005173 | TNNI2 | AMCD2B; DA2B; DA2B1; FSSV; fsTnI | troponin I2, fast skeletal type |
| TCMBANKGE006724 | REN | HNFJ2 | renin |
| TCMBANKGE011810 | PIEZO2 | C18orf30; C18orf58; DA3; DA5; DAIPT; FAM38B; FAM38B2; HsT748; HsT771; MWKS | piezo type mechanosensitive ion channel component 2 |
| TCMBANKGE007181 | WNK4 | PHA2B; PRKWNK4 | WNK lysine deficient protein kinase 4 |
| TCMBANKGE007800 | OSR1 | ODD | odd-skipped related transcription factor 1 |
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Dai SX Lab