搜索结果
疾病ID:TCMBANKDI010320
疾病名:Wolcott-Rallison syndrome
MeSH_Name:Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Immune System Diseases; Endocrine System Diseases
HPO_Name:-
UMLS_Name:Disease or Syndrome
DO_Name:genetic disease
疾病类型:disease
DisGeNET_Link:C0432217
MeSH_Link:C16; C18; C05; C20; C19
HPO_Link:-
UMLS_Link:T047
DO_Link:DOID:630
HERB_ID:HBDIS009401
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 |
|---|
| TCMBANKGE011918 | PPP1R15B | CREP; MSSGM2 | protein phosphatase 1 regulatory subunit 15B |
| TCMBANKGE000261 | INS | IDDM; IDDM1; IDDM2; ILPR; IRDN; MODY10; PNDM4 | insulin |
| TCMBANKGE001523 | EIF2S2 | EIF2; EIF2B; EIF2beta; PPP1R67; eIF-2-beta | eukaryotic translation initiation factor 2 subunit beta |
| TCMBANKGE007668 | EIF2S3 | EIF2; EIF2G; EIF2gamma; MEHMO; MRXSBRK; eIF-2gA | eukaryotic translation initiation factor 2 subunit gamma |
| TCMBANKGE009992 | ABCC8 | ABC36; HHF1; HI; HRINS; MRP8; PHHI; PNDM3; SUR; SUR1; SUR1delta2; TNDM2 | ATP binding cassette subfamily C member 8 |
| TCMBANKGE001381 | PAX4 | KPD; MODY9 | paired box 4 |
| TCMBANKGE001150 | EIF2S1 | EIF-2; EIF-2A; EIF-2alpha; EIF2; EIF2A | eukaryotic translation initiation factor 2 subunit alpha |
| TCMBANKGE000289 | EIF2AK3 | PEK; PERK; WRS | eukaryotic translation initiation factor 2 alpha kinase 3 |
| TCMBANKGE000197 | KCNJ11 | BIR; HHF2; IKATP; KIR6.2; MODY13; PHHI; PNDM2; TNDM3 | potassium inwardly rectifying channel subfamily J member 11 |
| TCMBANKGE005429 | ALPK3 | CMH27; MAK; MIDORI | alpha kinase 3 |
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Dai SX Lab