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HUMAN REPRODUCTIVE TECHNOLOGY ORDINANCE - SCHEDULE 2
Sex-linked Genetic Diseases
Remarks:
not yet in operation
[ss. 15(3)(a) & 46]
Addison's disease with cerebral sclerosis (Addison 病 (並有腦硬化))
Adrenoleucodystrophy (腎上腺白質營養不良)
Adrenal hypoplasia (腎上腺發育不良)
Agammaglobulinaemia, Bruton type (血球蛋白血病 (Bruton 型))
Agammaglobulinaemia, Swiss type (血球蛋白血病 (瑞士型))
Albinism, ocular (眼部白化病)
Albinism-deafness syndrome (白化病—耳聾綜合症)
Aldrich syndrome (Aldrich 綜合症)
Alport syndrome (Alport 綜合症)
Amelogenesis imperfecta, hypomaturation type (釉質生長不全 (成熟低下型))
Amelogenesis imperfecta, hypoplastic type (釉質生長不全 (發育不良型))
Anaemia, hereditary hypochromic (遺傳性低色數性貧血)
Angiokeratoma (Fabry's disease) (血管角質瘤 (Fabry 病))
Cataract, congenital (先天性白內障)
Cerebellar ataxia (小腦共濟失調)
Cerebral sclerosis, diffuse (擴散性腦硬化)
Charcot-Marie-Tooth peroneal muscular atrophy (Charcot-Marie-Tooth 腓骨肌萎縮症)
Choroideraemia (無脈絡膜症)
Choroidoretinal degeneration (脈絡膜視網膜變質)
Coffin-Lowry syndrome (Coffin-Lowry 綜合症)
Colour blindness, Deutan type (色盲 (綠色系列型))
Colour blindness, Protan type (色盲 (紅色系列型))
Diabetes insipidus, nephrogenic (腎原性尿崩症)
Diabetes insipidus, neurohypophyseal (尿崩症 (神經垂體型))
Dyskeratosis congenita (先天性角化不良)
Ectodermal dysplasia, anhidrotic (外胚層發育不全 (無汗型))
Ehlers-Danlos syndrome, type V (Ehlers-Danlos 綜合病 (第V類型))
Faciogenital dysplasia (Aarskog syndrome) (面生殖發育不全 (Aarskog 綜合症))
Focal dermal hypoplasia (X-linked dominant, male lethal) (局灶性皮膚發育不良 (與X染色體有關連的顯性，對男性而言可致死))
Glucose 6-phosphate dehydrogenase deficiency (葡糖6磷酸脫氫酶缺乏)
Glycogen storage disease, type VIII (糖原貯積症 (第VIII類型))
Gonadal dysgenesis (XY female type) (性腺發育不全 (XY女性類型))
Granulomatous disease (chronic) (慢性肉芽腫病)
Haemophilia A (血友病A)
Haemophilia B (血友病B)
Hydrocephalus (aqueduct stenosis) (腦積水 (中腦水管狹窄))
Hypophosphataemic rickets (低磷酸血性佝僂病)
Ichthyosis (steriod sulphatase deficiency) (魚鱗癬 (steriod sulphatase 缺乏))
Incontinentia pigmenti (X-linked dominant, male lethal) (色素失節症 (與X染色體有關連的顯性，對男性而言可致死))
Kallmann syndrome (Kallmann 綜合症)
Keratosis follicularis spinulosa (Spinulosa 毛囊角化病)
Lesch-Nyhan syndrome (hypoxanthine-guanine-phosphoribosyl transferase deficiency) (Lesch-Nyhan 綜合症 (次黃嘌呤—鳥嘌呤—磷酸核糖轉移缺乏))
Lowe (oculocerebrorenal) syndrome (Lowe (眼腦腎) 綜合症)
Macular dystrophy of the retina (視網膜黃斑營養不良)
Menkes syndrome (Menkes 綜合症)
Mental retardation, FMRI type (智力遲緩 (FMRI 型))
Mental retardation, FRAXE type (智力遲緩 (FRAXE 型))
Mental retardation, MRXI type (智力遲緩 (MRXI 型))
Microphthalmia with multiple anomalies (Lenz syndrome) (小眼症 (並有多種畸型) (Lenz 綜合症))
Mucopolysaccharidosis II (Hunter syndrome) (黏多糖貯積病II (Hunter 綜合症))
Muscular dystrophy, Becker type (肌營養不良 (Becker 型))
Muscular dystrophy, Duchenne type (肌營養不良 (Duchenne 型))
Muscular dystrophy, Emery-Dreifuss type (肌營養不良 (Emery-Dreifuss 型))
Myotubular myopathy (肌小管肌病)
Night blindness, congenital stationary (先天性靜止性夜盲症)
Norrie's disease (pseudoglioma) (Norrie's 病 (假性神經膠質瘤))
Nystagmus, oculomotor or 'jerky' (眼球震顫 (眼球運動的或抽動的))
Ornithine transcarbamylase deficiency (type I hyperammonaemia) (鳥氨酸胺甲轉移酶缺陷症(高氨血症第I類型))
Orofaciodigital syndrome (type I) (X-linked dominant, male lethal) (口—面—指 (趾) 綜合症(第I類型) (與X染色體有關連的顯性，對男性而言可致死))
Perceptive deafness, DNFZ type (感覺性聾症 (DNFZ 型))
Perceptive deafness, with ataxia and loss of vision (感覺性聾症 (並有共濟失調和喪失視力))
Phosphoglycerate kinase deficiency (磷酸甘油酸激酶缺乏)
Phosphoribosylpyrophosphate (PRPP) synthetase deficiency (磷酸核糖焦磷酸合成酶缺乏)
Reifenstein syndrome (Reifenstein 綜合症)
Retinitis pigmentosa (視網膜色素變性)
Retinoschisis (視網膜裂)
Spastic paraplegia (痙攣性痳痺)
Spinal muscular atrophy (脊椎肌萎縮)
Spondyloepiphyseal dysplasia tarda (遲發性脊椎骨發育不全)
Testicular feminization syndrome (睪丸女性化綜合症)
Thrombocytopenia, hereditary (遺傳性血小板減少症)
Thyroxine-binding globulin, absence or variants of (甲狀腺素—結合球蛋白缺乏或變種)
Xg blood group system (Xg 血型系統)