|
中文名称
|
英文名称
|
1
|
Aicardi-Goutières综合症
|
Aicardi-Goutières Syndrome (AGS)
|
2
|
Gitelman综合征
|
Gitelman Syndrome (GS)
|
3
|
Joubert综合征
|
Joubert Syndrome
|
4
|
Leber遗传性视神经病变
|
Leber Hereditary Optic Neuropathy (LHON)
|
5
|
Lennox-Gastaut综合征
|
Lennox-Gastaut Syndrome (LGS)
|
6
|
McCune-Albright综合征
|
Mccune-Albright Syndrome (MAS)
|
7
|
Rubinstein-Taybi综合征
|
Rubinstein-Taybi Syndrome(RSTS)
|
8
|
X-连锁高IgM综合症
|
X-Linked Hyper IgM Syndrome(HIGM1)
|
9
|
X连锁肾上腺脑白质营养不良
|
X-Linked Adrenoleukodystrophy (XLD)
|
10
|
X连锁鱼鳞病
|
Recessive X-Linked Ichthyosis(RXLI)
|
11
|
β-酮硫解酶缺乏症
|
Beta-Ketothiolase Deficiency (BKD)
|
12
|
白化病
|
Albinism
|
13
|
白塞病
|
Behcet's Syndrome (BS)
|
14
|
半乳糖血症
|
Galactosemia
|
15
|
伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病
|
Hereditary Multi-Infarct Dementia (Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts And Leukoencephalopathy, CADASIL)
|
16
|
苯丙酮尿症
|
Phenylketonuria (PKU)
|
17
|
丙酸血症
|
Propionic Acidemia (PA)
|
18
|
卟啉病
|
Porphyria
|
19
|
常染色体隐性多囊肾病
|
Autosomal Recessive Polycystic Kidney Disease (ARPKD)
|
20
|
成骨不全症(脆骨病)
|
Osteogenesis Imperfecta (OI)
|
21
|
脆性X染色体综合征
|
Fragile X Syndrome (FXS)
|
22
|
大疱性表皮松解症
|
Epidermolysis bullosa (EB)
|
23
|
低碱性磷酸酯酶血症
|
Hypophosphatasia
|
24
|
低磷性佝偻病
|
Hypophosphatemic Rickets
|
25
|
地中海贫血
|
Thalassemia
|
26
|
动脉肝脏发育不良综合征
|
Alagille Syndrome (AGS)
|
27
|
杜氏肌营养不良症
|
Duchenne Muscular Dystrophy (DMD)
|
28
|
遗传性软骨内骨发育不全
|
Multiple Epiphyseal Dysplasia(MED)
|
29
|
多发性骨髓瘤
|
Multiple Myeloma
|
30
|
多发性硬化
|
Multiple Sclerosis (MS)
|
31
|
法布雷病
|
Fabry Disease
|
32
|
范可尼贫血
|
Fanconi Anemia (FA)
|
33
|
非典型溶血性尿毒症综合征
|
Atypical Hemolytic-Uremic Syndrome (AHUS)
|
34
|
腓骨肌萎缩症
|
Charcot-Marie-Tooth Disease (CMT)
|
35
|
原发性肺动脉高压
|
Pulmonary Arterial Hypertension(PAH)
|
36
|
枫糖尿病
|
Maple Syrup Urine Disease (MSUD)
|
37
|
弗里曼-谢尔登氏综合征
|
Freeman-Sheldon Syndrome (FSS)
|
38
|
腹膜假性黏液瘤
|
PseudomyxomaPeritonei (PMP)
|
39
|
肝豆状核变性
|
Wilson Disease (WD)
|
40
|
高苯丙氨酸血症
|
Hyperphenylalaninemia
|
41
|
高前列腺素E综合征
(巴特综合征)
|
Hyperprostaglandin E Syndrome (Bartter Syndrome)
|
42
|
戈谢病
|
Gaucher Disease (GD)
|
43
|
歌舞伎面谱综合征
|
Kabuki Syndrome (KS)
|
44
|
共济失调-毛细血管扩张症
|
Ataxia-Telangiectasia (AT)
|
45
|
谷固醇血症
|
Sitosterolemia
|
46
|
骨髓增生异常综合征
|
Myelodysplastic Syndromes (MDS)
|
47
|
瓜氨酸血症
|
Citrullinemia
|
48
|
黑斑息肉综合征
|
Peutz-Jeghers Syndrome (PJS)
|
49
|
亨廷顿舞蹈症
|
Huntington Disease (HD)
|
50
|
真性红细胞增多症
|
Polycythemia Vera (PV)
|
51
|
肌萎缩侧索硬化症
|
Amyotrophic Lateral Sclerosis (ALS)
|
52
|
脊髓小脑性共济失调
|
Spinocerebellar Ataxia (SCA)
|
53
|
脊髓性肌萎缩症
|
Spinal Muscular Atrophy (SMA)
|
54
|
脊髓延髓肌肉萎缩症
(肯尼迪氏症)
|
Spinal And Bulbar Muscular Atrophy (Kennedy Disease)
|
55
|
季肋发育不全
|
Hypochondroplasia
|
56
|
家族性低血钾症
|
Familial Hypokalemia
|
57
|
家族性高胆固醇血症
|
Familial Hyperchylomicronemia(FH)
|
58
|
家族性高胰岛素性低血糖症
|
Hyperinsulinemic hypoglycemia, familial(HH)
|
59
|
甲基丙二酸血症
|
Methylmalonic Acidemia (MMA)
|
60
|
假性软骨发育不全
|
Pseudoachondroplasia
|
61
|
结节性硬化症
|
Tuberous Sclerosis Complex (TSC)
|
62
|
进行性骨化性纤维发育不良
|
Myositis ossificans progressiva (MOP)
|
63
|
进行性家族性肝内胆汁淤积症
|
Progressive Familial Intrahepatic Cholestasis
|
64
|
卡尔曼综合征
|
Kallmann Syndrome
|
65
|
克罗恩病
|
Crohn's Disease
|
66
|
克氏综合症
|
Klinefelter Syndrome (KS)
|
67
|
Laron综合征
|
Laron Syndrome
|
68
|
朗格汉斯细胞组织细胞增生症
|
Pulmonary Langerhans Cell Histiocytosis (PLCH)
|
69
|
酪氨酸血症
|
Tyrosinemia
|
70
|
雷特综合征
|
Rett Syndrome (RTS)
|
71
|
林岛综合征(VHL综合征)
|
Von Hippel–Lindau Disease (VHL Syndrome)
|
72
|
淋巴管肌瘤病
|
Lymphangioleiomyomatosis (LAM)
|
73
|
马凡综合征
|
Marfan Syndrome
|
74
|
猫叫综合征(5P-综合征)
|
Cri-du-chat Syndrome (5p- Syndrome)
|
75
|
面肩肱型肌营养不良症
|
Facioscapulohumeral Muscular Dystrophy
|
76
|
尼曼-匹克氏病
|
Niemann-Pick Disease (NPD)
|
77
|
尿素循环障碍
|
Urea Cycle Disorder (UCD)
|
78
|
努南综合征
|
Noonan Syndrome (NS)
|
79
|
庞贝病
|
Pompe Disease
|
80
|
佩梅病
|
Pelizaeus-Merzbacher Disease (PMD)
|
81
|
普拉德-威利综合征
(小胖威利综合征)
|
Prader-Willi Syndrome (PWS)
|
82
|
强直性肌营养不良
|
Myotonic Dystrophy (MD)
|
83
|
全羧化酶合成酶缺乏症
|
HolocarboxylaseSynthetase Deficiency
|
84
|
热纳综合征
|
Asphyxiating Thoracic Dystrophy (Jeune Syndrome)
|
85
|
溶酶体酸性脂肪酶缺乏症
|
Lysosomal Acid Lipase Deficiency
|
86
|
软骨发育不全
|
Achondroplasia
|
87
|
色素失禁症
|
IncontinentiaPigmenti(IP)
|
88
|
神经病-共济失调-色素性视网膜炎综合征
|
Neuropathy - Ataxia, And Retinitis Pigmentosa (NARP Syndrome)
|
89
|
神经纤维瘤病
|
Neurofibromatosis (NF)
|
90
|
生物素酶缺乏症
|
Biotinidase Deficiency
|
91
|
生长激素缺乏症
|
Growth Hormone Deficiency(GHD)
|
92
|
湿疹血小板减少伴免疫缺陷综合征
|
Wiskott-Aldrich Syndrome (WAS)
|
93
|
视神经脊髓炎
|
Neuromyelitis Optica (NMO)
|
94
|
视网膜母细胞瘤
|
Retinoblastoma
|
95
|
视网膜色素变性症
|
Retinitis Pigmentosa (RP)
|
96
|
四氢生物蝶呤缺乏症
|
Tetrahydrobiopterin Deficiency
|
97
|
糖原贮积病
|
Glycogen Storage Disease (GSD)
|
98
|
特纳综合征
|
Turner Syndrome
|
99
|
体质性肝功能不良性黄疸 (Gilbert综合征)
|
Gilbert's Syndrome (GS)
|
100
|
天使综合征
|
Angelman Syndrome (AS)
|
101
|
弯肢发育异常
|
Campomelic Dysplasia (CD)
|
102
|
威廉姆斯综合征
|
Williams Syndrome (WS)
|
103
|
无脑回畸形
|
Lissencephaly
|
104
|
戊二酸血症
|
Glutaric Acidemia (GA)
|
105
|
先天性Cajal氏间质细胞增生合并肠道神经元发育异常
|
Congenital Interstitial Cell Of Cajal Hyperplasia With Neuronal
|
106
|
先天性胆酸合成障碍
|
Inborn Errors Of Bile Acid Synthesis
|
107
|
先天性红细胞生成障碍性贫血
|
Congenital Dyserythropoietic Anemia (CDA)
|
108
|