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疾病ID:TCMBANKDI023959


疾病名:Pure Gonadal Dysgenesis, 46, XX


MeSH_Name:Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases


HPO_Name:-


UMLS_Name:Congenital Abnormality


DO_Name:disease of anatomical entity


疾病类型:disease


DisGeNET_Link:C0685837


MeSH_Link:C16; C13; C12; C19


HPO_Link:-


UMLS_Link:T019


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
TCMBANKGE000094 NR5A1 AD4BP; ELP; FTZ1; FTZF1; POF7; SF-1; SF1; SPGF8; SRXX4; SRXY3; hSF-1 nuclear receptor subfamily 5 group A member 1
TCMBANKGE014594 POLR3H C25; RPC22.9; RPC8 RNA polymerase III subunit H
TCMBANKGE007656 FSHR FSHR1; FSHRO; LGR1; ODG1 follicle stimulating hormone receptor
TCMBANKGE006588 BMP15 GDF9B; ODG2; POF4 bone morphogenetic protein 15
TCMBANKGE005217 NUP107 NPHS11; NUP84; ODG6; ODG6; GAMOS7 nucleoporin 107
TCMBANKGE009238 PSMC3IP GT198; HOP2; HUMGT198A; ODG3; TBPIP PSMC3 interacting protein