《罕見病目錄》是國家衛生健康委等6部門根據《罕見病目錄製訂工作程式》聯合制定的目錄。
截至2023年9月,中國共有207種罕見病納入目錄。
基本介紹
- 中文名:罕見病目錄
- 制定單位:國家衛生健康委等部門
發展歷程
批次目錄
第一批目錄
序號 | 中文名稱 | 英文名稱 |
---|---|---|
1 | 21-羥化酶缺乏症 | 21-Hydroxyulase Deficiency |
2 | 白化病 | Albinism |
3 | Alport 綜合徵 | Alport Syndrome |
4 | 肌萎縮側索硬化 | Amyotrophic Lateral Sclerosis |
5 | Angelman 氏症候群(天使綜合徵) | Angelman Syndrome |
6 | 精氨酸酶缺乏症 | Arginase Deficiency |
7 | 熱納綜合徵(窒息性胸腔失養症) | Asphyxiating Thoracic Dystrophy(Jeune Syndrome) |
8 | 非典型溶血性尿毒症 | Atypical Hemolytic Uremic Syndrome |
9 | 自身免疫性腦炎 | Autoimmune Encephalitis |
10 | 自身免疫性垂體炎 | Autoimmune Hypophysitis |
11 | 自身免疫性胰島素受體病 | Autoimmune Insulin Receptopathy(Type B insulin resistance) |
12 | β-酮硫解酶缺乏症 | Beta-ketothiolase Deficiency |
13 | 生物素酶缺乏症 | Biotinidase Deficiency |
14 | 心臟離子通道病 | Cardic Ion Channelopathies |
15 | 原發性肉鹼缺乏症 | Carnitine Deficiency |
16 | Castleman病 | Castleman Disease |
17 | 腓骨肌萎縮症 | Charcot-Marie-Tooth Disease |
18 | 瓜氨酸血症 | Citrullinemia |
19 | 先天性腎上腺發育不良 | Congenital Adrenal Hypoplasia |
20 | 先天性高胰島素性低血糖血症 | Congenital Hyperinsulinemic Hypoglycemia |
21 | 先天性肌無力綜合徵 | Congenital Myasthenic Syndrome |
22 | 先天性肌強直(非營養不良性肌強直綜合徵) | Congenital Myotonia Syndrome(Non-Dystrophic Myotonia, NDM) |
23 | 先天性脊柱側彎 | Congenital Scoliosis |
24 | 冠狀動脈擴張病 | Coronary Artery Ectasia |
25 | 先天性純紅細胞再生障礙性貧血 | Diamond-Blackfan Anemia |
26 | Erdheim-Chester病 | Erdheim-Chester Disease |
27 | 法布雷病 | Fabry Disease |
28 | 家族性地中海熱 | Familial Mediterranean Fever |
29 | 范可尼貧血 | Fanconi Anemia |
30 | 半乳糖血症 | Galactosemia |
31 | 戈謝病 | Gaucher's Disease |
32 | 全身型重症肌無力 | General Myathenic Gravis |
33 | Gitelman 綜合徵 | Gitelman Syndrome |
34 | 戊二酸血症I型 | Glutaric Acidemia Type I |
35 | 糖原累積病(I型、Ⅱ型) | Glycogen Storage Disease(Type I、II) |
36 | 血友病 | Hemophilia |
37 | 肝豆狀核變性 | Hepatolenticular Degeneration(Wilson Disease) |
38 | 遺傳性血管性水腫 | Hereditary Angioedema (HAE) |
39 | 遺傳性大皰性表皮鬆解症 | Hereditary Epidermolysis Bullosa |
40 | 遺傳性果糖不耐受症 | Hereditary Fructose Intolerance |
41 | 遺傳性低鎂血症 | Hereditary Hypomagnesemia |
42 | 遺傳性多發腦梗死性痴呆 | Hereditary Multi-infarct Dementia(Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy, CADASIL) |
43 | 遺傳性痙攣性截癱 | Hereditary Spastic Paraplegia |
44 | 全羧化酶合成酶缺乏症 | Holocarboxylase Synthetase Deficiency |
45 | 同型半胱氨酸血症 | Homocysteinemia |
46 | 純合子家族性高膽固醇血症 | Homozygous Hypercholesterolemia |
47 | 亨廷頓舞蹈病 | Huntington Disease |
48 | HHH綜合徵 | Hyperornithinaemia-Hyperammonaemia-Hhomocitrullinuria Syndrome |
49 | 高苯丙氨酸血症 | Hyperphenylalaninemia |
50 | 低鹼性磷酸酶血症 | Hypophosphatasia |
51 | 低磷性佝僂病 | Hypophosphatemic Rickets |
52 | 特發性心肌病 | Idiopathic Cardiomyopathy |
53 | 特發性低促性腺激素性性腺功能減退症 | Idiopathic Hypogonadotropic Hypogonadism |
54 | 特發性肺動脈高壓 | Idiopathic Pulmonary Arterial Hypertension |
55 | 特發性肺纖維化 | Idiopathic Pulmonary Fibrosis |
56 | IgG4相關性疾病 | IgG4 related Disease |
57 | 先天性膽汁酸合成障礙 | Inborn Errors of Bile Acid Synthesis |
58 | 異戊酸血症 | Isovaleric Acidemia |
59 | 卡爾曼綜合徵 | Kallmann Syndrome |
60 | 朗格漢斯組織細胞增生症 | Langerhans Cell Histiocytosis |
61 | 萊倫氏綜合徵 | Laron Syndrome |
62 | Leber遺傳性視神經病變 | Leber Hereditary Optic Neuropathy |
63 | 長鏈3-羥醯基輔酶A脫氫酶缺乏症 | Long Chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency |
64 | 淋巴管肌瘤病 | Lymphangioleiomyomatosis (LAM) |
65 | 賴氨酸尿蛋白不耐受症 | Lysine Urinary Protein Intolerance |
66 | 溶酶體酸性脂肪酶缺乏症 | Lysosomal Acid Lipase Deficiency |
67 | 楓糖尿症 | Maple Syrup Urine Disease |
68 | 馬凡綜合徵 | Marfan Syndrome |
69 | McCune-Albrigh綜合徵 | McCune-Albright Syndrome |
70 | 中鏈醯基輔酶A脫氫酶缺乏症 | Medium Chain Acyl-CoA Dehydrogenase Deficiency |
71 | 甲基丙二酸血症 | Methylmalonic Academia |
72 | 線粒體腦肌病 | Mitochodrial Encephalomyopathy |
73 | 黏多糖貯積症 | Mucopolysaccharidosis |
74 | 多灶性運動神經病 | Multi-Focal Motor Neurothy |
75 | 多種醯基輔酶A脫氫酶缺乏症 | Multiple Acyl-CoA Dehydrogenase Deficiency |
76 | 多發性硬化 | Multiple Sclerosis |
77 | 多系統萎縮 | Multiple System Atrophy |
78 | 肌強直性營養不良 | Myotonic Dystrophy |
79 | N-乙醯谷氨酸合成酶缺乏症 | NAGS Deficiency |
80 | 新生兒糖尿病 | Neonatal Diabetes Mellitus |
81 | 視神經脊髓炎 | Neuromyelitis Optica |
82 | 尼曼匹克病 | Niemann-Pick Disease |
83 | 非綜合徵性耳聾 | Non-Syndromic Deafness |
84 | Noonan綜合徵 | Noonan Syndrome |
85 | 鳥氨酸氨甲醯基轉移酶缺乏症 | Ornithine Transcarbamylase Deficiency |
86 | 成骨不全症(脆骨病) | Osteogenesis Imperfecta(Brittle Bone Disease) |
87 | 帕金森病(青年型、早髮型) | Parkinson Disease (Young-onset , Early-onset) |
88 | 陣發性睡眠性血紅蛋白尿 | Paroxysmal Nocturnal Hemoglobinuia |
89 | 黑斑息肉綜合徵 | Peutz-Jeghers Syndrome |
90 | 苯丙酮尿症 | Phenylketouria |
91 | POEMS綜合徵 | POEMS Syndrome |
92 | 卟啉病 | Porphyria |
93 | Prader-Willi綜合徵 | Prader-Willi Syndrome |
94 | 原發性聯合免疫缺陷 | Primary Combined Immune Deficiency |
95 | 原發性遺傳性肌張力不全 | Primary Hereditary Dystonia |
96 | 原發性輕鏈型澱粉樣變 | Primary Light Chain Amyloidosis |
97 | 進行性家族性肝內膽汁淤積症 | Progressive Familial Intrahepatic Cholestasis |
98 | 進行性肌營養不良 | Progressive Muscular Dystrophyies |
99 | 丙酸血症 | Propionic Acidemia |
100 | 肺泡蛋白沉積症 | Pulmonary Alveolar Proteinosis |
101 | 肺囊性纖維化 | Pulmonary Cystic Fibrosis |
102 | 視網膜色素變性症 | Retinitis Pigmentosa |
103 | 視網膜母細胞瘤 | Retinoblastoma |
104 | 重症先天性粒細胞缺乏症 | Severe Congenital Neutropenia |
105 | 嬰兒嚴重肌陣攣性癲癇(Dravet綜合徵) | Severe Myoclonic Epilepsy In Infaricy(Dravet Syndrome) |
106 | 鐮刀型細胞貧血病 | Sickle Cell Disease |
107 | Silver-Russell綜合徵 | Silver-Russell Syndrome |
108 | 谷固醇血症 | Sitosterolemia |
109 | 脊髓延髓肌萎縮症(甘迺迪病) | Spinal and Bulbar Muscular Atrophy(Kennedy Disease) |
110 | 脊髓性肌萎縮症 | Spinal Muscular Atrophy |
111 | 脊髓小腦性共濟失調 | Spinocerebellar Ataxia |
112 | 系統性硬化症 | Systemic Sclerosis |
113 | 四氫生物蝶呤缺乏症 | Tetrahydrobiopterin Deficiency |
114 | 結節性硬化症 | Tuberous Sclerosis Complex |
115 | 原發性酪氨酸血症 | Tyrosinemia |
116 | 極長鏈醯基輔酶A脫氫酶缺乏症 | Very Long Chain Acyl-CoA Dehydrogenase Deficiency |
117 | 威廉士綜合徵 | Williams Syndrome |
118 | 濕疹血小板減少伴免疫缺陷綜合徵 | Wiskott-Aldrich Syndrome |
119 | X-連鎖無丙種球蛋白血症 | X-linked Agammaglobulinemia |
120 | X-連鎖腎上腺腦白質營養不良 | X-linked Ldrenoleuko Dystrophy |
121 | X-連鎖淋巴增生症 | X-linked Lymphoproliferative Disease |
第二批目錄
序號 | 疾病名稱(中文) | 疾病名稱(英文) |
---|---|---|
1 | 軟骨發育不全 | Achondroplasia |
2 | 獲得性血友病 | Acquired hemophilia |
3 | 肢端肥大症 | Acromegaly |
4 | 成人斯蒂爾病 | Adult-onset Still disease |
5 | Alagille綜合徵 | Alagille syndrome |
6 | α-1-抗胰蛋白酶缺乏症 | Alpha-1-antitrypsin deficiency |
7 | ANCA相關性血管炎 | ANCA-associated vasculitis |
8 | Bardet-Biedl 綜合徵 | Bardet-Biedl syndrome |
9 | 白塞病/貝赫切特綜合徵 | Behçet's disease |
10 | 藍色橡皮皰樣痣 | Blue rubber bleb nevus |
11 | CDKL5缺乏症 | CDKL5-deficiency disorder |
12 | 無脈絡膜症 | Choroideremia |
13 | 慢性炎性脫髓鞘性多發性神經根神經病 | Chronic inflammatory demyelinating polyneuropathy |
14 | 腎透明細胞肉瘤 | Clear cell sarcoma of kidney |
15 | 冷凝集素病 | Cold agglutinin disease |
16 | 先天性膽道閉鎖 | Congenital biliary atresia |
17 | 先天性凝血因子VII缺乏症 | Congenital factor VII deficiency |
18 | 冷吡啉(冷炎素)相關周期性綜合徵/ NLRP3相關自身炎症性疾病 | Cryopyrin associated periodic syndrome/ NLRP3-associated systemic autoinflammatory disease |
19 | 皮膚神經內分泌癌(梅克爾細胞癌) | Cutaneous neuroendocrine carcinoma(Merkel cell carcinoma) |
20 | 皮膚T細胞淋巴瘤 | Cutaneous T-cell lymphomas |
21 | 胱氨酸貯積症 | Cystinosis |
22 | 隆突性皮膚纖維肉瘤 | Dermatofibrosarcoma protuberans |
23 | 嗜酸性粒細胞性胃腸炎 | Eosinophilic gastroenteritis |
24 | 上皮樣肉瘤 | Epithelioid sarcoma |
25 | 面肩肱型肌營養不良症 | Facioscapulohumeral muscular dystrophy |
26 | 家族性噬血細胞淋巴組織細胞增生症 | Familial hemophagocytic lymphohistiocytosis |
27 | 家族性腺瘤性息肉病 | Familial adenomatous polyposis |
28 | 進行性骨化性纖維發育不良 | Fibrodysplasia ossificans progressiva |
29 | 脆性X綜合徵 | Fragile X syndrome |
30 | 神經節苷脂貯積症 | Gangliosidosis |
31 | 胃腸胰神經內分泌腫瘤 | Gastroenteropancreatic neuroendocrine neoplasm |
32 | 胃腸間質瘤 | Gastrointestinal stromal tumor |
33 | 泛發性膿皰型銀屑病 | Generalized pustular psoriasis |
34 | 遺傳性甲狀旁腺功能減退症 | Genetic hypoparathyroidism |
35 | 巨細胞動脈炎 | Giant cell arteritis |
36 | 骨巨細胞瘤 | Giant cell tumor of bone |
37 | 血小板無力症 | Glanzmann thrombasthenia |
38 | 膠質母細胞瘤 | Glioblastoma |
39 | 高林綜合徵 | Gorlin syndrome |
40 | 化膿性汗腺炎 | Hidradenitis suppurativa |
41 | 早老症 | Hutchinson-Gilford progeria syndrome |
42 | 炎性肌纖維母細胞瘤 | Inflammatory myofibroblastic tumor |
43 | Leber先天性黑矇 | Leber congenital amaurosis |
44 | Lennox-Gastaut 綜合徵 | Lennox-Gastaut syndrome |
45 | 角膜緣幹細胞缺乏症 | Limbal stem cell deficiency |
46 | 惡性高熱 | Malignant hyperthermia |
47 | 惡性胸膜間皮瘤 | Malignant pleural mesothelioma |
48 | 黑色素瘤 | Melanoma |
49 | 異染性腦白質營養不良 | Metachromatic leukodystrophy |
50 | 單基因非綜合徵性肥胖 | Monogenic non-syndromic obesity |
51 | 多發性內分泌腺瘤病 | Multiple endocrine neoplasia |
52 | 發作性睡病 | Narcolepsy |
53 | 神經母細胞瘤 | Neuroblastoma |
54 | 神經纖維瘤病 | Neurofibromatosis |
55 | 神經元蠟樣脂褐質沉積症 | Neuronal ceroid lipofuscinosis |
56 | 神經營養性角膜炎 | Neurotrophic keratitis |
57 | 骨肉瘤 | Osteosarcoma |
58 | 天皰瘡 | Pemphigus |
59 | 新生兒持續肺動脈高壓 | Persistent pulmonary hypertension of the newborn |
60 | 嗜鉻細胞瘤 | Pheochromocytoma |
61 | PIK3CA相關過度生長綜合徵 | PIK3CA related overgrowth syndrome |
62 | 真性紅細胞增多症 | Polycythaemia vera |
63 | 原發性膽汁性膽管炎 | Primary biliary cholangitis |
64 | 原發性生長激素缺乏症 | Primary growth hormone deficiency |
65 | 原發性胰島素樣生長因子-1缺乏症 | Primary IGF1 deficiency |
66 | 原發性免疫缺陷 | Primary immunodeficiency |
67 | 原發性骨髓纖維化 | Primary myelofibrosis |
68 | 原發性硬化性膽管炎 | Primary sclerosing cholangitis |
69 | 進行性纖維化性間質性肺疾病 | Progressive fibrosing interstitial lung disease |
70 | 復發性心包炎 | Recurrent pericarditis |
71 | 早產兒視網膜病 | Retinopathy of prematurity |
72 | Rett綜合徵 | Rett syndrome |
73 | 短腸綜合徵 | Short bowel syndrome |
74 | 全身型幼年特發性關節炎 | Systemic juvenile idiopathic arthritis |
75 | 系統性肥大細胞增多症 | Systemic mastocytosis |
76 | 大動脈炎/多發性大動脈炎 | Takayasu arteritis |
77 | 腱鞘巨細胞瘤/色素沉著絨毛結節性滑膜炎 | Tenosynovial giant cell tumor/Pigmented villonodular synovitis |
78 | 地中海貧血(重型) | Thalassemia major |
79 | 血栓性血小板減少性紫癜 | Thrombotic thrombocytopenic purpura |
80 | 轉甲狀腺素蛋白澱粉樣變性 | Transthyretin amyloidosis |
81 | 腫瘤壞死因子受體相關周期性綜合徵 | Tumor necrosis factor receptor associated periodic syndrome |
82 | 腫瘤相關骨軟化症 | Tumor-induced osteomalacia |
83 | Von Hippel-Lindau綜合徵 | Von Hippel-Lindau syndrome |
84 | 血管性血友病Ⅲ型 | Von Willebrand disease type3 |
85 | 華氏巨球蛋白血症/淋巴漿細胞淋巴瘤 | Waldenström macroglobulinemia/ Lymphoplasmacytic lymphoma |
86 | West綜合徵/嬰兒痙攣綜合徵 | West syndrome/Infantile spasms syndrome |