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疾病ID:TCMBANKDI021337
疾病名:Osteogenesis imperfecta, dominant perinatal lethal
MeSH_Name:Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
HPO_Name:-
UMLS_Name:Disease or Syndrome; Congenital Abnormality
DO_Name:genetic disease; disease of anatomical entity
疾病类型:disease
DisGeNET_Link:C0268358
MeSH_Link:C16; C17; C05
HPO_Link:-
UMLS_Link:T047; T019
DO_Link:DOID:630; 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 |
|---|
| TCMBANKGE008131 | PPIB | B; CYP-S1; CYPB; HEL-S-39; OI9; SCYLP | peptidylprolyl isomerase B |
| TCMBANKGE000160 | COL2A1 | ANFH; AOM; COL11A3; SEDC; STL1 | collagen type II alpha 1 chain |
| TCMBANKGE004740 | CRTAP | CASP; LEPREL3; OI7; P3H5 | cartilage associated protein |
| TCMBANKGE008225 | COL1A2 | EDSARTH2; EDSCV; OI4 | collagen type I alpha 2 chain |
| TCMBANKGE000712 | COL1A1 | CAFYD; EDSARTH1; EDSC; OI1; OI2; OI3; OI4 | collagen type I alpha 1 chain |
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Dai SX Lab