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中文Pelger-Huet Anomaly (PHA)
Alias:
Pelger-Huët Anomaly
Pha
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佩尔格-胡特异常，又称佩尔格-胡特异常，与骨软骨发育不良和肌营养不良有关。与佩尔格-胡特异常有关的重要基因是LBR（Lamin B Receptor），其相关通路/超级通路包括细胞周期、有丝分裂和高尔基体至内质网反向运输。附属组织包括中性粒细胞和骨髓，相关表型包括中性粒细胞异常和染色体分离异常
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