Nevoid Hypermelanosis, Linear And Whorled |
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Eosinophilia |
OMIM:614323 |
Immunodeficiency 88 |
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Eosinophilia |
OMIM:619630 |
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 |
Carbimazole Sensitivity |
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Drug-induced agranulocytosis |
OMIM:212060 |
Eosinophil Peroxidase Deficiency |
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Abnormal eosinophil morphology |
OMIM:261500 |
Eosinophilia, Familial |
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Leukocytosis, Eosinophilia, Anemia, Thrombocytopenia |
OMIM:131400 |
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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Leukocytosis, Eosinophilia |
ORPHA:26137 |
Neutropenia, Severe Congenital, 1, Autosomal Dominant |
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Thrombocytosis, Neutropenia, Monocytosis, Congenital agranulocytosis, Anemia, Acute monocytic leu... |
OMIM:202700 |
Immunodeficiency 7 |
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Hypereosinophilia |
OMIM:615387 |
Acute Myelomonocytic Leukemia |
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Leukocytosis, Eosinophilia, Anemia, Thrombocytopenia |
ORPHA:517 |
Macrosomia Adiposa Congenita |
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Eosinophilia |
OMIM:248100 |
Eosinophilopenia |
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Decreased eosinophil count |
OMIM:131430 |
Hypereosinophilic Syndrome, Idiopathic |
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Myeloproliferative disorder, Eosinophilia, Splenomegaly |
OMIM:607685 |
Myalgia-Eosinophilia Syndrome Associated With Tryptophan |
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Eosinophilia, Lymphopenia |
ORPHA:2582 |
Kimura Disease |
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Eosinophilia |
ORPHA:482 |
Generalized Eruptive Histiocytosis |
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Leukemia, Hypereosinophilia, Histiocytosis |
ORPHA:157991 |
Halothane Hepatitis |
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Eosinophilia |
OMIM:234350 |
Chronic Myeloid Leukemia |
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Thrombocytosis, Abnormal basophil morphology, Leukocytosis, Abnormal granulocyte morphology, Sple... |
ORPHA:521 |
Undritz Anomaly |
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Hypersegmentation of neutrophil nuclei |
OMIM:191500 |
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 |
Candidiasis, Familial, 2 |
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Hypereosinophilia |
OMIM:212050 |
Hyper-Ige Recurrent Infection Syndrome 2, Autosomal Recessive |
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Eosinophilia |
OMIM:243700 |
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1 |
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Eosinophilia |
OMIM:253600 |
Autoimmune Lymphoproliferative Syndrome |
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Elevated proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells, Neutropenia in ... |
OMIM:601859 |
Eosinophilic Fasciitis |
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Abnormal eosinophil morphology, Eosinophilia |
ORPHA:3165 |
Hyper-Ige Recurrent Infection Syndrome 3, Autosomal Recessive |
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Eosinophilia |
OMIM:618282 |
Omenn Syndrome |
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B lymphocytopenia, Hypoplasia of the thymus, Anemia, Splenomegaly, Severe B lymphocytopenia, Thro... |
OMIM:603554 |
Neutropenia, Severe Congenital, 2, Autosomal Dominant |
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B lymphocytopenia, Neutropenia, Monocytosis |
OMIM:613107 |
O'Sullivan-Mcleod Syndrome |
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Eosinophilia |
ORPHA:99965 |
T-B+ Severe Combined Immunodeficiency Due To Il-7Ralpha Deficiency |
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Neutropenia, Decreased proportion of CD3-positive T cells, Hepatosplenomegaly, Lymphocytosis, Aut... |
ORPHA:169154 |
Cinca Syndrome |
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Leukocytosis, Hepatosplenomegaly, Eosinophilia, Anemia |
OMIM:607115 |
Intellectual Developmental Disorder With Speech Delay, Dysmorphic Facies, And T-Cell Abnormalities |
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Eosinophilia |
OMIM:618092 |
Neutropenia, Nonimmune Chronic Idiopathic, Of Adults |
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Acute myeloid leukemia, Neutropenia |
OMIM:607847 |
Autosomal Dominant Severe Congenital Neutropenia |
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Acute lymphoblastic leukemia, Neutropenia, Monocytosis, Leukemia, Acute myeloid leukemia, Lymphop... |
ORPHA:486 |
Autoimmune Lymphoproliferative Syndrome, Type Iia |
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Increased B cell count, Elevated proportion of CD4-negative, CD8-negative, alpha-beta regulatory ... |
OMIM:603909 |
Hyper-Ige Recurrent Infection Syndrome 4B, Autosomal Recessive |
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Eosinophilia |
OMIM:618523 |
Hyper-Ige Recurrent Infection Syndrome 1, Autosomal Dominant |
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Eosinophilia |
OMIM:147060 |
Idiopathic Acute Eosinophilic Pneumonia |
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Abnormal eosinophil morphology |
ORPHA:724 |
Immunodeficiency 60 And Autoimmunity |
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Pancytopenia, Decreased basophil count, Decreased proportion of memory B cells, Splenomegaly |
OMIM:618394 |
Immunodeficiency 25 |
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Eosinophilia, T lymphocytopenia, Autoimmune hemolytic anemia |
OMIM:610163 |
Systemic Mastocytosis With Associated Hematologic Neoplasm |
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Leukocytosis, Chronic lymphatic leukemia, Normocytic anemia, Normochromic anemia, Chronic myelomo... |
ORPHA:98849 |
Autoinflammation, Immune Dysregulation, And Eosinophilia |
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Hepatosplenomegaly, Eosinophilia |
OMIM:618999 |
Immunodeficiency 49 |
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Eosinophilia, Lymphopenia |
OMIM:617237 |
Severe Combined Immunodeficiency Due To Complete Rag1/2 Deficiency |
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Abnormal B cell count, Decreased proportion of CD3-positive T cells, Hepatosplenomegaly, Abnormal... |
ORPHA:331206 |
T-B+ Severe Combined Immunodeficiency Due To Cd3Delta/Cd3Epsilon/Cd3Zeta |
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Decreased proportion of CD3-positive T cells, Hepatosplenomegaly, Eosinophilia, Lymphopenia |
ORPHA:169160 |
Immunodysregulation, Polyendocrinopathy, And Enteropathy, X-Linked |
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Neutropenia, Coombs-positive hemolytic anemia, Anemia, Autoimmune thrombocytopenia, Thrombocytope... |
OMIM:304790 |
Eosinophilic Gastroenteritis |
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Leukocytosis, Eosinophilia, Anemia |
ORPHA:2070 |
Roifman Syndrome |
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Hepatosplenomegaly, Eosinophilia |
ORPHA:353298 |
Omenn Syndrome |
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Leukocytosis, Abnormal lymphocyte morphology, Anemia, Splenomegaly, Eosinophilia |
ORPHA:39041 |
Roifman Syndrome |
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Eosinophilia, Splenomegaly |
OMIM:616651 |
Hereditary Folate Malabsorption |
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Pancytopenia, Thrombocytopenia, Eosinophilia, Megaloblastic anemia |
ORPHA:90045 |
Combined Immunodeficiency Due To Zap70 Deficiency |
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Absence of CD8-positive T cells, Hepatosplenomegaly, Lymphocytosis, Autoimmune thrombocytopenia, ... |
ORPHA:911 |
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due To Adenosine Deaminase Deficiency |
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B lymphocytopenia, Reduced red cell adenosine deaminase level, Splenomegaly, Aplasia of the thymu... |
OMIM:102700 |
Idiopathic Chronic Eosinophilic Pneumonia |
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Leukocytosis, Hypereosinophilia |
ORPHA:2902 |
Pgm3-Cdg |
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Abnormal CD4:CD8 ratio, Neutropenia, Abnormal proportion of CD8-positive T cells, Leukopenia, Neu... |
ORPHA:443811 |
Autoinflammation With Arthritis And Dyskeratosis |
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Hypereosinophilia, Autoimmune hemolytic anemia, Splenomegaly |
OMIM:617388 |
Netherton Syndrome |
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Hypereosinophilia |
OMIM:256500 |
Allergic Bronchopulmonary Aspergillosis |
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Abnormal eosinophil morphology |
ORPHA:1164 |
Loeffler Endocarditis |
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Eosinophilia |
ORPHA:75566 |
Aspergillosis |
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Eosinophilia, Neutropenia |
ORPHA:1163 |
Iga Pemphigus |
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Eosinophilia, Cutaneous abscess |
ORPHA:555905 |
Igg4-Related Aortitis |
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Hypereosinophilia |
ORPHA:449400 |
Immunodeficiency 23 |
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Neutropenia, Abscess, Lymphopenia, Eosinophilia, Hemolytic anemia |
OMIM:615816 |
Immunoskeletal Dysplasia With Neurodevelopmental Abnormalities |
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Eosinophilia, Lymphopenia |
OMIM:617425 |
Immunodeficiency 89 And Autoimmunity |
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Decreased eosinophil count, Hypochromic microcytic anemia |
OMIM:619632 |
Drug Reaction With Eosinophilia And Systemic Symptoms |
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Eosinophilia, Lymphocytosis |
ORPHA:139402 |
Cyclic Neutropenia |
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Perianal abscess, Lymphopenia, Cyclic neutropenia, Thrombocytopenia, Tooth abscess, Decreased eos... |
ORPHA:2686 |
Autoimmune Lymphoproliferative Syndrome |
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Increased B cell count, Elevated proportion of CD4-negative, CD8-negative, alpha-beta regulatory ... |
ORPHA:3261 |
Cystic Echinococcosis |
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Peritoneal abscess, Abscess, Eosinophilia, Splenic cyst |
ORPHA:400 |
Autosomal Dominant Hyper-Ige Syndrome |
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Eosinophilia |
ORPHA:2314 |
Mucoepithelial Dysplasia, Hereditary |
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Eosinophilia |
OMIM:158310 |
Eosinophilic Granulomatosis With Polyangiitis |
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Eosinophilia |
ORPHA:183 |
Angiostrongyliasis |
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Hypereosinophilia |
ORPHA:74 |
Wiskott-Aldrich Syndrome |
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Absent microvilli on the surface of peripheral blood lymphocytes, Impaired lymphocyte transformat... |
OMIM:301000 |
Late-Onset Isolated Acth Deficiency |
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Macrocytic anemia, Eosinophilia, Normocytic anemia |
ORPHA:199299 |
Alveolar Echinococcosis |
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Anemia, Abnormal spleen morphology, Eosinophilia, Cutaneous abscess, Liver abscess |
ORPHA:284 |
Skeletal Dysplasia-T-Cell Immunodeficiency-Developmental Delay Syndrome |
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Hypereosinophilia, Decreased proportion of CD4-positive helper T cells, Decreased proportion of C... |
ORPHA:508533 |
Scleroderma |
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Hypereosinophilia |
ORPHA:801 |
Idiopathic Hypereosinophilic Syndrome |
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Leukocytosis, Thrombocytosis, Anemia, Splenomegaly, Myeloproliferative disorder, Hepatosplenomega... |
ORPHA:3260 |
Thrombocytopenia-Absent Radius Syndrome |
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Leukocytosis, Anemia, Hepatosplenomegaly, Thrombocytopenia, Eosinophilia |
OMIM:274000 |
Incontinentia Pigmenti |
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Leukocytosis, Eosinophilia |
OMIM:308300 |
Igg4-Related Pachymeningitis |
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Eosinophilia |
ORPHA:449427 |
Incontinentia Pigmenti |
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Eosinophilia |
ORPHA:464 |
Coccidioidomycosis |
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Granuloma, Abnormality of the spleen, Eosinophilia, Abscess |
ORPHA:228123 |
Lymphatic Filariasis |
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Hypereosinophilia |
ORPHA:2035 |
Igg4-Related Submandibular Gland Disease |
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Eosinophilia |
ORPHA:449432 |
Igg4-Related Kidney Disease |
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Eosinophilia |
ORPHA:449395 |
Igg4-Related Ophthalmic Disease |
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Eosinophilia |
ORPHA:449563 |
Sarcoidosis |
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Leukopenia, Increased T cell count, Anemia, Thrombocytopenia, Eosinophilia, Hemolytic anemia |
ORPHA:797 |
Wiskott-Aldrich Syndrome |
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Neutropenia, Acute leukemia, Hypoplasia of the thymus, Chronic leukemia, Abnormal platelet morpho... |
ORPHA:906 |
Tropical Endomyocardial Fibrosis |
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Eosinophilia, Splenomegaly |
ORPHA:75565 |
Viss Syndrome |
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Hypereosinophilia |
OMIM:619472 |
Cushing Disease |
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Leukocytosis, Lymphopenia, Decreased eosinophil count |
ORPHA:96253 |
Dermatomyositis |
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Abnormal eosinophil morphology |
ORPHA:221 |
Cushing Syndrome Due To Ectopic Acth Secretion |
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Leukocytosis, Lymphopenia, Decreased eosinophil count |
ORPHA:99889 |
Microcephaly, Facial Dysmorphism, Renal Agenesis, And Ambiguous Genitalia Syndrome |
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OMIM:618142 |