X-连锁隐性遗传性脊髓延髓型肌萎缩
X-linked spinal and bulbar muscular atrophy
伴皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Cerebral autosomal dominant arteriopathy with subc
伴皮质下梗死及白质脑病常染色体显性遗传性脑动脉病
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
常染色体显性遗传性病变
autosomal dominant disorder
常染色体显性遗传性多囊肾病
autosomal dominant polycystic kidney disease
Autosomal dominant polycentric kidney disease
常染色体隐性遗传性脑动脉病伴皮质下梗死和白质脑病
cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
常染色体隐性遗传性早发型帕金森综合征
autosomal recessive early-onset Parkinsonism
家族性遗传性淀粉样变性NOS
Neuropathic heredofamilial amyloidosis
色素异常症,对称性,遗传性
Dyschromatosis symmetrica hereditaria
遗传性传导障碍
hereditary cochleosaccular degeneration
隐性遗传性营养不良性大疱性表皮松解症
Recessive dystrophic epidermolysis ullosa
Ⅳ型遗传性血色病
hereditary hemochromatosis type
Leber’s遗传性视神经病变
Leber’s hereditary optic neuropathy
Leber遗传性视神经病
LHON
Leber’s hereditary optic neuropathy
leber hereditary optic neuropathy
Leber遗传性视神经病变
Leber’s hereditary optic neuropathy
leber hereditary optic neuropathy