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嘌呤代谢异常

Disorder of purine metabolism

ORPHA:79191疾病组

相关基因 13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
ADAadenosine deaminaseORPHA:277
ADSLadenylosuccinate lyaseORPHA:46
APRTadenine phosphoribosyltransferaseORPHA:976
ATIC5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolaseORPHA:250977
DGUOKdeoxyguanosine kinaseORPHA:279934
HPRT1hypoxanthine phosphoribosyltransferase 1ORPHA:510
ITPAinosine triphosphataseORPHA:457375
MOCOSmolybdenum cofactor sulfuraseORPHA:93602
PAICSphosphoribosylaminoimidazole carboxylase and phosphoribosylaminoimidazolesuccinocarboxamide synthaseORPHA:633099
PNPpurine nucleoside phosphorylaseORPHA:760
PRPS1phosphoribosyl pyrophosphate synthetase 1ORPHA:99014
UMODuromodulinORPHA:88950
XDHxanthine dehydrogenaseORPHA:93601

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)