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Autosomal Dominant Cerebellar Ataxia type 1
Autosomal Dominant Cerebellar Ataxia Type I
Autosomal Dominant Cerebellar Ataxia Type II
Autosomal dominant Compelling Helio-Ophthalmic Outburst
Autosomal Dominant Congenital Stationary Night Blindness
Autosomal Dominant Cortical Cerebellar Atrophy
Autosomal Dominant Cortical Myoclonus and Epilepsy
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy
Autosomal dominant Familial Neurohypophyseal Diabetes Insipidus
Autosomal Dominant Hemolytic Uremic Syndrome
Autosomal Dominant Hereditary Spastic Paraplegia
Autosomal Dominant Hypophosphatemic Rickets
Autosomal dominant hypophosphatemic rickets
Autosomal Dominant Ichthyosis Vulgaris
Autosomal Dominant Lamellar Ichthyosis
Autosomal Dominant Lateral Temporal Lobe Epilepsy
Autosomal Dominant Macular Degeneration
Autosomal Dominant Macular Dystrophy
autosomal dominant medullary cystic kidney disease
Autosomal Dominant Motor System Degeneration
Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy
Autosomal Dominant Neurohypophyseal Diabetes Insipidus
Autosomal dominant nocturnal frontal lobe epilepsy
Autosomal Dominant Non-Syndromal Hearing Impairment
Autosomal Dominant Non-Syndromic Hearing Loss
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更新时间:2024/11/16 11:31:48