Nevoid Hypermelanosis, Linear And Whorled |
|
Eosinophilia |
OMIM:614323 |
Immunodeficiency 88 |
|
Eosinophilia |
OMIM:619630 |
Eosinophilia, Familial |
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Leukocytosis, Eosinophilia, Myocardial eosinophilic infiltration, Anemia, Thrombocytopenia |
OMIM:131400 |
Myeloproliferative Disorder, Chronic, With Eosinophilia |
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Myeloproliferative disorder, Eosinophilia |
OMIM:131440 |
Neutropenia, Lethal Congenital, With Eosinophilia |
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Eosinophilia, Neutropenia |
OMIM:257100 |
Hypereosinophilic Syndrome, Idiopathic |
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Hepatomegaly, Splenomegaly, Restrictive cardiomyopathy, Myeloproliferative disorder, Eosinophilia... |
OMIM:607685 |
Eosinophil Peroxidase Deficiency |
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Eosinophil nuclear hypersegmentation |
OMIM:261500 |
Neutropenia, Severe Congenital, 1, Autosomal Dominant |
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Acute monocytic leukemia, Eosinophilia, Monocytosis, Congenital agranulocytosis, Thrombocytosis, ... |
OMIM:202700 |
Ichthyosis-Prematurity Syndrome |
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Eosinophilia |
ORPHA:88621 |
Immunodeficiency 11B With Atopic Dermatitis |
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Eosinophilia |
OMIM:617638 |
Juvenile Temporal Arteritis |
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Eosinophilia, Leukocytosis |
ORPHA:26137 |
Ethanolaminosis |
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Cardiomegaly |
OMIM:227150 |
Acute Myelomonocytic Leukemia |
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Anemia, Eosinophilia, Thrombocytopenia, Leukocytosis |
ORPHA:517 |
Immunodeficiency 7 |
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Hypereosinophilia |
OMIM:615387 |
Macrosomia Adiposa Congenita |
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Eosinophilia |
OMIM:248100 |
Myalgia-Eosinophilia Syndrome Associated With Tryptophan |
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Eosinophilia, Lymphopenia |
ORPHA:2582 |
Eosinophilopenia |
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Decreased eosinophil count |
OMIM:131430 |
Generalized Eruptive Histiocytosis |
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Histiocytosis, Leukemia, Hypereosinophilia |
ORPHA:157991 |
Immunodeficiency 103, Susceptibility To Fungal Infections |
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Abnormal proportion of CD8-positive T cells, Abnormal B cell count, Hypereosinophilia, Abnormal n... |
OMIM:212050 |
Halothane Hepatitis |
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Eosinophilia |
OMIM:234350 |
Kimura Disease |
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Eosinophilia |
ORPHA:482 |
Loeffler Endocarditis |
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Myocardial fibrosis, Aortic valve stenosis, Abnormal morphology of the chordae tendinae of the mi... |
ORPHA:75566 |
Autoimmune Lymphoproliferative Syndrome |
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Neutropenia in presence of anti-neutropil antibodies, Hepatomegaly, Coombs-positive hemolytic ane... |
OMIM:601859 |
Wells Syndrome |
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Eosinophilia |
ORPHA:901 |
Esophagitis, Eosinophilic, 1 |
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Eosinophilia |
OMIM:610247 |
Esophagitis, Eosinophilic, 2 |
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Eosinophilia |
OMIM:613412 |
Omenn Syndrome |
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Hepatomegaly, Splenomegaly, Eosinophilia, Hypoplasia of the thymus, Severe B lymphocytopenia, B l... |
OMIM:603554 |
Cardiomyopathy, Dilated, 1I |
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Dilated cardiomyopathy, Cardiomegaly |
OMIM:604765 |
Immunodeficiency 97 With Autoinflammation |
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Neutropenia in presence of anti-neutropil antibodies, Lymphopenia, Hemophagocytosis, Splenomegaly... |
OMIM:619802 |
Cinca Syndrome |
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Anemia, Eosinophilia, Hepatosplenomegaly, Leukocytosis |
OMIM:607115 |
T-B+ Severe Combined Immunodeficiency Due To Il-7Ralpha Deficiency |
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Lymphopenia, Lymphocytosis, Hepatosplenomegaly, Eosinophilia, Autoimmune thrombocytopenia, T lymp... |
ORPHA:169154 |
Hyper-Ige Recurrent Infection Syndrome 3, Autosomal Recessive |
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Eosinophilia |
OMIM:618282 |
Autoimmune Lymphoproliferative Syndrome, Type Iia |
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Neutropenia in presence of anti-neutropil antibodies, Hepatomegaly, Coombs-positive hemolytic ane... |
OMIM:603909 |
Eosinophilic Fasciitis |
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Eosinophilia, Abnormal eosinophil morphology |
ORPHA:3165 |
Roifman Syndrome |
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Hepatomegaly, Splenomegaly, Eosinophilia, Ventricular septal defect, Noncompaction cardiomyopathy |
OMIM:616651 |
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1 |
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Eosinophilia |
OMIM:253600 |
Intellectual Developmental Disorder With Speech Delay, Dysmorphic Facies, And T-Cell Abnormalities |
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Eosinophilia |
OMIM:618092 |
Hyper-Ige Recurrent Infection Syndrome 1, Autosomal Dominant |
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Eosinophilia, Cutaneous abscess |
OMIM:147060 |
Roifman Syndrome |
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Eosinophilia, Hepatosplenomegaly, Noncompaction cardiomyopathy |
ORPHA:353298 |
Autoinflammation, Immune Dysregulation, And Eosinophilia |
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Eosinophilia, Hepatosplenomegaly |
OMIM:618999 |
Hyper-Ige Recurrent Infection Syndrome 4B, Autosomal Recessive |
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Eosinophilia |
OMIM:618523 |
Severe Combined Immunodeficiency Due To Complete Rag1/2 Deficiency |
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Abnormal T cell count, Hepatomegaly, Lymphopenia, Hepatosplenomegaly, Eosinophilia, Abnormal B ce... |
ORPHA:331206 |
Autosomal Dominant Severe Congenital Neutropenia |
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Lymphopenia, Eosinophilia, Monocytosis, Aplastic anemia, Acute lymphoblastic leukemia, Neutropeni... |
ORPHA:486 |
Omenn Syndrome |
|
Hepatomegaly, Leukocytosis, Splenomegaly, Eosinophilia, Abnormal lymphocyte morphology, Anemia |
ORPHA:39041 |
Peeling Skin Syndrome 1 |
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Eosinophilia |
OMIM:270300 |
Systemic Mastocytosis With Associated Hematologic Neoplasm |
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Abnormal mast cell morphology, Hepatomegaly, Neutrophilia, Splenomegaly, Leukocytosis, Myeloproli... |
ORPHA:98849 |
O'Sullivan-Mcleod Syndrome |
|
Eosinophilia |
ORPHA:99965 |
T-B+ Severe Combined Immunodeficiency Due To Cd3Delta/Cd3Epsilon/Cd3Zeta |
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Eosinophilia, Hepatosplenomegaly, Lymphopenia, Decreased proportion of CD3-positive T cells |
ORPHA:169160 |
Immunodeficiency 25 |
|
Autoimmune hemolytic anemia, Eosinophilia, T lymphocytopenia |
OMIM:610163 |
Immunodeficiency 49 |
|
Eosinophilia, Lymphopenia |
OMIM:617237 |
Severe Combined Immunodeficiency With Sensitivity To Ionizing Radiation |
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Lymphopenia, Hepatomegaly, Splenomegaly, Aplasia of the thymus, Abnormally low T cell receptor ex... |
OMIM:602450 |
Immunodysregulation, Polyendocrinopathy, And Enteropathy, X-Linked |
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Coombs-positive hemolytic anemia, Eosinophilia, Autoimmune thrombocytopenia, Neutropenia, Anemia,... |
OMIM:304790 |
Idiopathic Acute Eosinophilic Pneumonia |
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Abnormal eosinophil morphology |
ORPHA:724 |
Eosinophilic Gastroenteritis |
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Eosinophilia, Anemia, Leukocytosis |
ORPHA:2070 |
Autoinflammation With Arthritis And Dyskeratosis |
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Autoimmune hemolytic anemia, Hepatomegaly, Hypereosinophilia, Splenomegaly |
OMIM:617388 |
Hyper-Ige Recurrent Infection Syndrome 2, Autosomal Recessive |
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Eosinophilia, Decreased proportion of CD4-positive helper T cells, Reduced natural killer cell count |
OMIM:243700 |
Combined Immunodeficiency Due To Zap70 Deficiency |
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Lymphocytosis, Eosinophilia, Hepatosplenomegaly, Autoimmune thrombocytopenia, Decreased proportio... |
ORPHA:911 |
Hereditary Folate Malabsorption |
|
Megaloblastic anemia, Eosinophilia, Thrombocytopenia, Pancytopenia |
ORPHA:90045 |
Pgm3-Cdg |
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Abnormal proportion of CD8-positive T cells, Lymphopenia, Neutropenia in presence of anti-neutrop... |
ORPHA:443811 |
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due To Adenosine Deaminase Deficiency |
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Hepatomegaly, Lymphopenia, Splenomegaly, Aplasia of the thymus, Severe B lymphocytopenia, Eosinop... |
OMIM:102700 |
Idiopathic Chronic Eosinophilic Pneumonia |
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Hypereosinophilia, Leukocytosis |
ORPHA:2902 |
Cystic Echinococcosis |
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Hepatomegaly, Eosinophilia, Abscess, Peritoneal abscess, Splenic cyst, Abnormal heart morphology |
ORPHA:400 |
Aspergillosis |
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Eosinophilia, Neutropenia |
ORPHA:1163 |
Netherton Syndrome |
|
Hypereosinophilia |
OMIM:256500 |
Eosinophilic Granulomatosis With Polyangiitis |
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Abnormal pericardium morphology, Eosinophilia, Endocarditis, Myocarditis, Hypertrophic cardiomyop... |
ORPHA:183 |
Drug Reaction With Eosinophilia And Systemic Symptoms |
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Eosinophilia, Lymphocytosis, Myocarditis |
ORPHA:139402 |
Immunodeficiency 23 |
|
Lymphopenia, Eosinophilia, Abscess, Hemolytic anemia, Neutropenia |
OMIM:615816 |
Autoimmune Lymphoproliferative Syndrome |
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Autoimmune hemolytic anemia, Abnormal proportion of CD8-positive T cells, Hepatomegaly, Lymphopen... |
ORPHA:3261 |
Obesity-Colitis-Hypothyroidism-Cardiac Hypertrophy-Developmental Delay Syndrome |
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Cardiomegaly |
ORPHA:88643 |
Mucoepithelial Dysplasia, Hereditary |
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Cor pulmonale, Eosinophilia |
OMIM:158310 |
Igg4-Related Aortitis |
|
Hypereosinophilia |
ORPHA:449400 |
Allergic Bronchopulmonary Aspergillosis |
|
Abnormal eosinophil morphology |
ORPHA:1164 |
Iga Pemphigus |
|
Cutaneous abscess, Eosinophilia |
ORPHA:555905 |
Immunoskeletal Dysplasia With Neurodevelopmental Abnormalities |
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Eosinophilia, Lymphopenia |
OMIM:617425 |
Autosomal Dominant Hyper-Ige Syndrome |
|
Eosinophilia |
ORPHA:2314 |
Alveolar Echinococcosis |
|
Cutaneous abscess, Abnormal pericardium morphology, Abnormal spleen morphology, Eosinophilia, Ane... |
ORPHA:284 |
Scleroderma |
|
Interstitial cardiac fibrosis, Pericarditis, Hypereosinophilia, Myocarditis |
ORPHA:801 |
Cyclic Neutropenia |
|
Lymphopenia, Cyclic neutropenia, Perianal abscess, Tooth abscess, Thrombocytopenia, Decreased eos... |
ORPHA:2686 |
Skeletal Dysplasia-T-Cell Immunodeficiency-Developmental Delay Syndrome |
|
Hepatomegaly, Lymphopenia, T lymphocytopenia, Decreased proportion of CD8-positive T cells, Mitra... |
ORPHA:508533 |
Cardiomyopathy, Familial Hypertrophic 27 |
|
Right ventricular hypertrophy, Concentric hypertrophic cardiomyopathy, Endocardial fibroelastosis... |
OMIM:618052 |
Idiopathic Hypereosinophilic Syndrome |
|
Neutrophilia, Leukocytosis, Splenomegaly, Myeloproliferative disorder, Hepatosplenomegaly, Eosino... |
ORPHA:3260 |
Angiostrongyliasis |
|
Hypereosinophilia |
ORPHA:74 |
Late-Onset Isolated Acth Deficiency |
|
Eosinophilia, Normocytic anemia, Macrocytic anemia |
ORPHA:199299 |
Thrombocytopenia-Absent Radius Syndrome |
|
Atrial septal defect, Leukocytosis, Atrioventricular canal defect, Hepatosplenomegaly, Eosinophil... |
OMIM:274000 |
Immunodeficiency 89 And Autoimmunity |
|
Decreased eosinophil count, Hypochromic microcytic anemia |
OMIM:619632 |
Wiskott-Aldrich Syndrome |
|
Lymphopenia, Eosinophilia, Absent microvilli on the surface of peripheral blood lymphocytes, Decr... |
OMIM:301000 |
Tropical Endomyocardial Fibrosis |
|
Hepatomegaly, Right ventricular cardiomyopathy, Splenomegaly, Restrictive cardiomyopathy, Eosinop... |
ORPHA:75565 |
Attrv122I Amyloidosis |
|
Cardiac amyloidosis, Aortic valve stenosis, Restrictive cardiomyopathy, Left ventricular hypertro... |
ORPHA:85451 |
Incontinentia Pigmenti |
|
Eosinophilia |
ORPHA:464 |
Incontinentia Pigmenti |
|
Eosinophilia, Leukocytosis |
OMIM:308300 |
Coccidioidomycosis |
|
Eosinophilia, Abscess, Abnormality of the spleen, Granuloma, Pericarditis |
ORPHA:228123 |
Congenital Tricuspid Valve Dysplasia |
|
Tricuspid valve prolapse, Right atrial enlargement, Anomalous pulmonary venous return, Hepatomega... |
ORPHA:555874 |
Igg4-Related Pachymeningitis |
|
Eosinophilia |
ORPHA:449427 |
Sickle Cell Anemia |
|
Hepatomegaly, Leukocytosis, Splenomegaly, Hemolytic anemia, Target cells, Cardiomegaly, Increased... |
OMIM:603903 |
Igg4-Related Kidney Disease |
|
Eosinophilia, Pericarditis, Enlarged kidney |
ORPHA:449395 |
Gaucher Disease, Type Iiic |
|
Mitral stenosis, Aortic valve calcification, Hepatomegaly, Splenomegaly, Mitral valve calcificati... |
OMIM:231005 |
Lymphatic Filariasis |
|
Hypereosinophilia |
ORPHA:2035 |
Igg4-Related Submandibular Gland Disease |
|
Eosinophilia |
ORPHA:449432 |
Sarcoidosis |
|
Hepatomegaly, Eosinophilia, Leukopenia, Hemolytic anemia, Anemia, Thrombocytopenia, Increased T c... |
ORPHA:797 |
Aorta Coarctation |
|
Bicuspid aortic valve, Hypoplastic left heart, Aortic valve atresia, Tetralogy of Fallot, Abnorma... |
ORPHA:1457 |
Igg4-Related Ophthalmic Disease |
|
Eosinophilia |
ORPHA:449563 |
Viss Syndrome |
|
Double outlet right ventricle, Atrial septal defect, Right ventricular hypertrophy, Ventricular s... |
OMIM:619472 |
Wiskott-Aldrich Syndrome |
|
Lymphopenia, Abnormal eosinophil morphology, Hypoplasia of the thymus, Hemolytic anemia, Microcyt... |
ORPHA:906 |
Cushing Disease |
|
Lymphopenia, Decreased eosinophil count, Leukocytosis |
ORPHA:96253 |
Dermatomyositis |
|
Pericarditis, Abnormal eosinophil morphology, Myocarditis |
ORPHA:221 |
Cushing Syndrome Due To Ectopic Acth Secretion |
|
Lymphopenia, Decreased eosinophil count, Leukocytosis |
ORPHA:99889 |