| 疾病名称 |
别名 |
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| Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema |
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Dehydrated Hereditary Stomatocytosis
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Hereditary Xerocytosis
|
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Xerocytosis, Hereditary
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Pshk1
|
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Pseudohyperkalemia Edinburgh
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Dehydrated Hereditary Stomatocytosis With Or Without Pseudohyperkalemia And/Or Perinatal Edema
|
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DHS1
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Dhs
|
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Hereditary Desiccytosis
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Dehydrated Hereditary Stomatocytosis 1
|
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Desiccytosis, Hereditary
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Pseudohyperkalemia, Familial, 1, Due To Red Cell Leak
|
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Pseudohyperkalemia Familial 1, Due To Red Cell Leak
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Desiccytosis Hereditary
|
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Xerocytosis Hereditary
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Familial Pseudohyperkalemia 1 Due To Red Cell Leak
|
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Stomatocytosis, Dehydrated, Hereditary, With/Without Pseudohyperkalemia And/Or Perinatal Edema
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Xerocytosis
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| Lymphatic Malformation 6 |
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LMPHM6
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Generalized Lymphatic Dysplasia Of Fotiou
|
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Lymphedema, Hereditary, Iii
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Lymphedema, Hereditary, Iii, Formerly
|
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Lmph3, Formerly
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Lmph3
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Lymphedema, Hereditary, 3
|
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| Hereditary Stomatocytosis |
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Hereditary Stomatocytic Disease
|
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| Immune Hydrops Fetalis |
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Ihf
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Immune Hf
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Immune Fetal Edema
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Immune Fetal Hydrops
|
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| Hemolytic Anemia |
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Anemia, Hemolytic
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Anemia Hemolytic
|
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Anaemia Due To Other Disorders Of Glutathione Metabolism
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Chronic Non Spherocytic Anaemia
|
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G6pd - [Glucose-6-Phosphate Dehydrogenase Deficiency] Anaemia
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Anaemia Due To Glucose-6-Phosphate Dehydrogenase Deficiency
|
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Glucose-6-Phosphate Dehydrogenase Deficiency With Anaemia
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Glucose-6-Phosphate Dehydrogenase Deficiency Anaemia
|
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Favism Anaemia
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Haemolytic Anaemia Due Tog6pd Deficiency
|
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Favism
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Pentose Phosphate Pathway Disorder Anaemia
|
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Anaemia Due To Pentose Phosphate Pathway Defect
|
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| Glutamate-Cysteine Ligase Deficiency |
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Gamma-Glutamylcysteine Synthetase Deficiency
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Hemolytic Anemia Due To Gamma-Glutamylcysteine Synthetase Deficiency
|
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Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due To
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| Anemia, Congenital Dyserythropoietic, Type Ia |
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Congenital Dyserythropoietic Anemia Type I
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Cda I
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CDAN1A
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Congenital Dyserythropoietic Anemia Type 1
|
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Congenital Dyserythropoietic Anemia Type Ia
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Congenital Dyserythropoietic Anemia, Type I
|
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Anemia, Congenital Dyserythropoietic, Type I
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Cda Type 1
|
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Cda Type I
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Cda Ia
|
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Dyserythropoietic Anemia, Congenital Type 1
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Anemia, Congenital Dyserythropoietic, Type 1a
|
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Dyserythropoietic Anemia, Congenital, Type Ia
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Cda, Type Ia
|
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Congenital Dyserythropoietic Anaemia Type 1
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Congenital Dyserythropoietic Anaemia Type I
|
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Anemia, Dyserythropoietic, Congenital Type 1
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Type I Congenital Dyserythropoietic Anemia
|
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Anemia, Congenital Dyserythropoietic, 1a
|
Anemia, Dyserythropoietic, Congenital, Type Ia
|
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| Hereditary Lymphedema Ia |
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Lmph1a
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Lymphedema, Hereditary, Ia
|
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Milroy Disease
|
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| Primary Lymphedema |
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| Pyruvate Kinase Deficiency Of Red Cells |
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Pyruvate Kinase Deficiency
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Pk Deficiency
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Pyruvate Kinase Deficiency Of Erythrocyte
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Hemolytic Anemia Due To Red Cell Pyruvate Kinase Deficiency
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Pyruvate Kinase Deficiency Of Erythrocytes
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Pkd
|
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PKRD
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Hereditary Non-Spherocytic Hemolytic Anemia Due To Pyruvate Kinase Deficiency
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Hnsha
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Pyruvate Kinase-Deficient Hemolytic Anemia
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Red Cell Pyruvate Kinase Deficiency
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Deficiency Of Pyruvate Kinase
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Anemia, Hemolytic, Congenital Nonspherocytic
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| Congenital Nonspherocytic Hemolytic Anemia |
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Hereditary Non-Spherocytic Hemolytic Anemia
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Hereditary Nonspherocytic Hemolytic Anemia
|
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Anemia, Hemolytic, Congenital Nonspherocytic
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Congenital Nonspherocytic Hemolytic Anaemia
|
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Hereditary Nonspherocytic Hemolytic Anaemia
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Hnsha
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| Varicose Veins |
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Varices
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Varix
|
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Venous Ectasia
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Venous Varices
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Varicosity
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| Cerebral Cavernous Malformations |
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Cerebral Cavernous Malformation
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Cavernous Malformations Of Cns And Retina
|
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Cerebral Cavernous Malformation 1
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Cavernous Angiomatous Malformations
|
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Cerebral Capillary Malformations
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CCM
|
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Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated With Cerebral Capillary Malformations
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Familial Cavernous Angioma
|
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Cavernous Angioma
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Familial Cerebral Cavernous Malformation
|
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Cerebral Cavernous Malformations 1
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Cavernous Angioma, Familial
|
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Cam
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Cerebral Cavernous Malformations-1
|
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Cavernoma
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Central Nervous System Cavernous Hemangioma
|
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Cerebral Cavernous Hemangioma
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Familial Cavernous Hemangioma
|
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Familial Cavernous Malformation
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Familial Cerebral Cavernous Angioma
|
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Intracerebral Cavernous Hemangioma
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CCM1
|
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Cavernous Hemangioma Of The Brain
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Cerebral Cavernoma
|
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Cerebral Cavernous Malformations, Type 1
|
Hemangioma, Cavernous, Central Nervous System
|
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Hemangioma, Cavernous
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Angioma, Cavernous
|
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| Hennekam Syndrome |
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Hennekam Lymphangiectasia Lymphedema Syndrome
|
Hennekam Lymphangiectasia-Lymphedema Syndrome
|
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Lymphedema-Lymphangiectasia-Intellectual Disability Syndrome
|
Lymphedem-Lymphangiectasia-Intellectual Disability Syndrome
|
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Intestinal Lymphagiectasia Lymphedema Intellectual Deficit Syndrome
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Lymphangiectasies And Lymphedema Hennekam Type
|
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Generalized Lymphatic Dysplasia
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Intestinal Lymphagiectasia-Lymphedema-Mental Retardation Syndrome
|
|
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| Arthrogryposis, Distal, Type 3 |
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Gordon Syndrome
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DA3
|
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Distal Arthrogryposis Type 3
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Arthrogryposis Multiplex Congenita, Distal, Type Iia
|
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Camptodactyly, Cleft Palate, And Clubfoot
|
Camptodactyly-Cleft Palate-Clubfoot Syndrome
|
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Distal Arthrogryposis Multiplex Congenita Type Iia
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Arthrogryposis Distal Type 3
|
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Distal Arthrogryposis Type Iia
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Arthrogryposis, Distal, 3
|
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Pseudohypoaldosteronism, Type Ii
|
|
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| Erythrocytosis, Familial, 8 |
|
Diphosphoglycerate Mutase Deficiency Of Erythrocyte
|
ECYT8
|
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Bisphosphoglycerate Mutase Deficiency
|
Bisphosphoglyceromutase Deficiency
|
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Bpgm Deficiency
|
Dpgm Deficiency
|
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Deficiency Of Bisphosphoglycerate Mutase
|
Familial Erythrocytosis 8
|
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Hemolytic Anemia Due To Diphosphoglycerate Mutase Deficiency
|
Erythrocytosis Due To Bisphosphoglycerate Mutase Deficiency
|
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Erythrocytosis, Familial, Type 8
|
|
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| Overhydrated Hereditary Stomatocytosis |
|
Ohs
|
Potassium Sodium Disorder Of Erythrocyte
|
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OHST
|
Stomatocytosis I
|
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Potassium-Sodium Disorder Of Erythrocyte
|
Stomatocytosisiohst
|
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Hereditary, Overhydrated, Cation-Leak Stomatocytosis
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Overhydrated Cation Leak Stomatocytosis
|
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Stomatocytosis, Overhydrated Hereditary
|
|
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| Hereditary Spherocytosis |
|
Congenital Spherocytic Hemolytic Anemia
|
Spherocytic Anemia
|
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Congenital Spherocytosis
|
Spherocytosis, Type 1
|
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Minkowski Chauffard Syndrome
|
Hs
|
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Minkowski-Chauffard Disease
|
Minkowski-Chauffard Syndrome
|
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Spherocytosis Hereditary
|
Spherocytosis, Hereditary
|
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Anemia, Hereditary Spherocytic Hemolytic
|
|
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| Arthrogryposis, Distal, Type 5 |
|
Oculomelic Amyoplasia
|
Distal Arthrogryposis Type 5
|
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Distal Arthrogryposis Type Iib
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DA5
|
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Arthrogryposis With Oculomotor Limitation And Electroretinal Abnormalities
|
Daiib
|
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Distal Arthrogryposis Type 2b
|
Arthrogryposis-Oculomotor Limitation-Electroretinal Anomalies Syndrome
|
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Distal Arthrogryposis With Ophthalmoplegia
|
Arthrogryposis- Oculomotor Limitation-Electroretinal Anomalies Syndrome
|
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Arthrogryposis, Distal, Type Iib
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Da2b
|
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Freeman-Sheldon Syndrome Variant
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Sheldon-Hall Syndrome
|
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Arthogryposis With Oculomotor Limitation And Electroretinal Abnormalities
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Arthrogryposis Ophthalmoplegia Retinopathy
|
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Arthrogryposis, Distal, 5
|
Arthrogryposis, Distal, Type 2b
|
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| Hereditary Elliptocytosis |
|
Congenital Elliptocytosis
|
Ovalocytosis
|
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Elliptocytosis, Hereditary
|
He
|
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Elliptocytosis Hereditary
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Congenital Ovalocytosis
|
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Elliptocytosis
|
Hereditary Elliptocytosis With Infantile Poikilocytosis
|
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Hereditary Ovalocytosis
|
Oval Erythrocytosis
|
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He - [Hereditary Elliptocytosis]
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Elliptocytosis Anaemia
|
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| Anemia, Congenital Dyserythropoietic, Type Ii |
|
Congenital Dyserythropoietic Anemia Type Ii
|
CDAN2
|
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Cda Ii
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Hereditary Erythroblastic Multinuclearity With Positive Acidified-Serum Test
|
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Cda Type Ii
|
Congenital Dyserythropoietic Anemia Type 2
|
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Hereditary Erythroblastic Multinuclearity With A Positive Acidified-Serum Test
|
Sec23b-Cdg
|
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Congenital Dyserythropoietic Anemia, Type Ii
|
Dyserythropoietic Anemia, Hempas Type
|
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Hempas
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Cda Type 2
|
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Dyserythropoietic Anemia, Congenital, Type Ii
|
Cda, Type Ii
|
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Congenital Dyserythropoietic Anaemia Type 2
|
Congenital Dyserythropoietic Anaemia Type Ii
|
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Anemia, Dyserythropoietic, Congenital Type 2
|
Hempas Anemia
|
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Dyserythropoietic Anemia, Congenital Type 2
|
Anemia, Congenital Dyserythropoietic, 2
|
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Dyserythropoietic Anemia Hempas Type
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Anemia, Dyserythropoietic Congenital, Type Ii
|
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Anemia, Dyserythropoietic, Congenital, Type Ii
|
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| Anemia, Congenital Dyserythropoietic, Type Iv |
|
CDAN4
|
Congenital Dyserythropoietic Anemia Type Iv
|
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Congenital Dyserythropoietic Anemia Type 4
|
Cda Iv
|
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Cda Due To Klf1 Mutation
|
Cda Type 4
|
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Cda Type Iv
|
Congenital Dyserythropoietic Anemia Due To Klf1 Mutation
|
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Cda, Type Iv
|
Dyserythropoietic Anemia, Congenital, Type Iv
|
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Congenital Dyserythropoietic Anaemia Due To Klf1 Mutation
|
Congenital Dyserythropoietic Anaemia Type 4
|
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Congenital Dyserythropoietic Anaemia Type Iv
|
Anemia, Congenital Dyserythropoietic, 4
|
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Anemia, Dyserythropoietic Congenital, Type Iv
|
Anemia, Dyserythropoietic, Congenital, Type Iv
|
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| Hereditary Lymphedema |
|
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| Malaria |
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Malaria, Susceptibility To
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Malaria, Resistance To
|
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Malaria, Cerebral
|
Cerebral Malaria
|
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Malaria, Severe, Susceptibility To
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Malaria, Severe, Resistance To
|
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Malaria, Cerebral, Susceptibility To
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Induced Malaria
|
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Malaria, Vivax, Protection Against
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Malaria, Severe
|
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Malaria, Cerebral, Reduced Risk Of
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Malaria, Protection Against
|
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Resistance To Malaria Due To G6pd Deficiency
|
Malaria Due To G6pd Deficiency
|
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Malarial Encephalitis
|
CM
|
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Malaria Cerebral
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Susceptibility To Malaria
|
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Acute Pernicious Fever
|
Aestivo-Autumnal Fever
|
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Aestivo Autumnal Malaria
|
Chagres Fever
|
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Continued Malaria Fever
|
Estivo-Autumnal Fever
|
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Estivo-Autumnal Malaria
|
Estivo-Autumnal Malarial Fever
|
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Falciparum Fever
|
Malignant Tertian Fever
|
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Malignant Tertian Malaria
|
Pernicious Intermittent Fever
|
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Pernicious Malaria
|
Quotidian Malaria
|
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Subtertian Fever
|
Subtertian Malaria Fever
|
|
Subtertian Malignant Tertian Malaria
|
Tropical Malaria
|
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Algid Malaria
|
Bilious Haemoglobinuric Fever
|
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Black Water Fever
|
Blackwater Fever
|
|
Malarial Blackwater Fever
|
Severe Malarial Falciparum
|
|
West African Fever
|
Malarial Haematinuria
|
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Haemoglobinuric Fever
|
Haemoglobinuric Malaria
|
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Severe Plasmodium Falciparum Malaria
|
Malarial Haemoglobinuria
|
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Malarial Haematuria
|
Falciparum Malaria [Malignant Tertian]
|
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Malaria Tropica
|
Malarial Shock
|
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Chagres Virus Disease
|
Malignant Malaria
|
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Mtm - [Malignant Tertian Malaria]
|
Tm -[Malignant Tertian Malaria]
|
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Panama Fever
|
St - [Subtertian Malaria]
|
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Malarial Quotidian
|
Benign Tertian Malaria
|
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Tertian Ague
|
Vivax Fever
|
|
Plasmodium Vivax Malaria Nos
|
Btm - [Benign Tertian Malaria]
|
|
Bt - [Benign Tertian Malaria]
|
Vivax Malaria
|
|
Benign Tertian Vivax Malaria
|
Tertian Malaria
|
|
Quartan Malaria
|
Quartan Ague
|
|
Quartan Fever
|
Plasmodium Malariae Malaria Nos
|
|
Quartan Malarial
|
Malaria By Plasmodium Malariae
|
|
Malariae Malaria
|
Ovale Tertian Malaria
|
|
Plasmodium Ovale Fever
|
Malaria Fever By Plasmodium Ovale
|
|
Ovale Malaria
|
Malaria By Plasmodium Ovale
|
|
Malarial Ovale
|
Marsh Fever
|
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Remittent Congestive Fever
|
Coastal Fever
|
|
Remittent Gastric Fever
|
Miasmatic Fever
|
|
Congestive Remittent Fever
|
Intermittent Fever
|
|
Jungle Fever
|
Paludism
|
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Cameroon Fever
|
Ague
|
|
Corsican Fever
|
Intermittent Bilious Fever
|
|
Disease Due To Plasmodiidae
|
Malarial Fever
|
|
Plasmodiosis
|
Remittent Fever
|
|
Roman Fever
|
Malaria Fever Nos
|
|
Malaria Nos
|
Paludal Fever
|
|
Clinically Diagnosed Malaria
|
Clinically Diagnosed Malaria Without Parasitological Confirmation
|
|
Congestive Fever
|
Malarial Cachexia
|
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Marsh Cachexia
|
Paludal Cachexia
|
|
Recurrent Malaria
|
Remittent Malaria
|
|
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| Hereditary Lymphedema I |
|
Lymphedema
|
Hereditary Lymphedema Type I
|
|
Congenital Primary Lymphedema
|
Lmph1
|
|
Milroy Disease
|
Nonne-Milroy Lymphedema
|
|
Pcl
|
Lymphedema Hereditary Type 1
|
|
|
| Congenital Hemolytic Anemia |
|
Anemia Hemolytic Congenital
|
Anemia, Hemolytic, Congenital
|
|
Congenital Hemolytic Anaemia
|
Hereditary Hemolytic Anaemia
|
|
Hereditary Hemolytic Anemia
|
|
|
| Erythrocytosis, Familial, 7 |
|
ECYT7
|
Erythrocytosis 7
|
|
Familial Erythrocytosis 7
|
Erythrocytosis, Alpha-Globin Type
|
|
Polycythemia, Alpha-Globin Type
|
Alpha-Globin Type Erythrocytosis
|
|
Alpha-Globin Type Polycythemia
|
|
|
| Lymphedema-Distichiasis Syndrome |
|
Lymphedema With Distichiasis
|
Lymphedema-Distichiasis Syndrome With Renal Disease And Diabetes Mellitus
|
|
LPHDST
|
Distichiasis-Lymphedema Syndrome
|
|
Lymphedema Distichiasis Syndrome
|
Hereditary Lymphedema-Distichiasis Syndrome
|
|
Lymphedema Distichiasis
|
|
|
| Glucosephosphate Dehydrogenase Deficiency |
|
G6pd Deficiency
|
Glucose-6-Phosphate Dehydrogenase Deficiency
|
|
Deficiency Of Glucose-6-Phosphate Dehydrogenase
|
Glucose 6 Phosphate Dehydrogenase Deficiency
|
|
Deficiency Of G-6pd
|
G6pdd
|
|
|
| Osteogenesis Imperfecta, Type Iii |
|
Osteogenesis Imperfecta Type Iii
|
OI3
|
|
Oi, Type Iii
|
Osteogenesis Imperfecta Type 3
|
|
Oi Type Iii
|
Oi Type 3
|
|
Progressive Deforming Osteogenesis Imperfecta
|
Severe Osteogenesis Imperfecta
|
|
Osteogenesis Imperfecta, Progressively Deforming, With Normal Sclerae
|
Progressively Deforming Osteogenesis Imperfecta With Normal Sclera
|
|
Osteogenesis Imperfecta, Progressively Deforming With Normal Sclerae
|
Progressively Deforming Oi
|
|
Osteogenesis Imperfecta 3
|
Oi-Iii
|
|
Progressively Deforming Osteogenesis Imperfecta With Normal Sclerae
|
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|
