罕见病知识库 RareSeen

性发育异常

Difference of sex development

ORPHA:90771疾病组

别名

DSD

相关基因 23来自下位疾病

Orphanet 未在本条目上直接标注致病基因。下表由本组所属的下位疾病汇总而来,「来源条目」列给出基因实际标注在哪一个 ORPHA 条目上。

基因名称来源条目
AMHanti-Mullerian hormoneORPHA:2856
AMHR2anti-Mullerian hormone receptor type 2ORPHA:2856
ARandrogen receptorORPHA:90797
ATRXATRX chromatin remodelerORPHA:847
CYP11A1cytochrome P450 family 11 subfamily A member 1ORPHA:168558
DHHdesert hedgehog signaling moleculeORPHA:168563
DHX37DEAH-box helicase 37ORPHA:251510
GATA4GATA binding protein 4ORPHA:251510
HHAThedgehog acyltransferaseORPHA:1422
HSD17B3hydroxysteroid 17-beta dehydrogenase 3ORPHA:752
MAP3K1mitogen-activated protein kinase kinase kinase 1ORPHA:251510
MCM9minichromosome maintenance 9 homologous recombination repair factorORPHA:444048
NR5A1nuclear receptor subfamily 5 group A member 1ORPHA:2138
PPP2R3Cprotein phosphatase 2 regulatory subunit B''gammaORPHA:1770
RSPO1R-spondin 1ORPHA:85112
SOX3SRY-box transcription factor 3ORPHA:393
SOX9SRY-box transcription factor 9ORPHA:2138
SRD5A2steroid 5 alpha-reductase 2ORPHA:753
SRYsex determining region YORPHA:2138
TSPYL1TSPY like 1ORPHA:168593
WT1WT1 transcription factorORPHA:347
WWOXWW domain containing oxidoreductaseORPHA:251510
ZFPM2zinc finger protein, FOG family member 2ORPHA:251510

外部标识与链接

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本页数据来源

  • 疾病定义、同义词、基因、表型、流行病学:Orphanet(CC BY 4.0)
  • 中文病名:Orphanet 中文包,冻结于 2020-06-01
  • 表型中文标签:HPO 简体中文翻译(CHPO 上游成果)