| Diseases |
Alias |
|
| Immunodeficiency 32a |
|
Mendelian Susceptibility To Mycobacterial Diseases Due To Partial Irf8 Deficiency
|
IMD32A
|
|
Immunodeficiency 32a, Mycobacteriosis, Autosomal Dominant
|
Mendelian Susceptibility To Mycobacterial Diseases Due To Partial Interferon Regulatory Factor 8 Deficiency
|
|
Msmd Due To Partial Interferon Regulatory Factor 8 Deficiency
|
Msmd Due To Partial Irf8 Deficiency
|
|
Irf8 Deficiency, Autosomal Dominant
|
Cd11c-Positive/Cd1c-Positive Dendritic Cell Deficiency, Autosomal Dominant
|
|
Autosomal Dominant Cd11c-Positive/Cd1c-Positive Dendritic Cell Deficiency
|
Autosomal Dominant Immunodeficiency 32a, Mycobacteriosis
|
|
Autosomal Dominant Irf8 Deficiency
|
Immunodeficiency, Type 32a
|
|
|
| Immunodeficiency 32b |
|
IMD32B
|
Immunodeficiency 32b, Monocyte And Dendritic Cell Deficiency, Autosomal Recessive
|
|
Immunodeficiency 32b, Monocyte, Dendritic Cell, And Natural Killer Cell Deficiency, Autosomal Recessive
|
Irf8 Deficiency, Autosomal Recessive
|
|
Epstein-Barr Virus Chronic Infection By
|
Epstein-Barr Virus, Susceptibility To Chronic Infection By
|
|
Autosomal Recessive Irf8 Deficiency
|
Chronic Epstein-Barr Virus Infection Syndrome
|
|
Caebv Syndrome
|
Chronic Ebv Infection Syndrome
|
|
Autosomal Recessive Monocyte And Dendritic Cell Deficiency
|
Immunodeficiency, Type 32b
|
|
Monocyte And Dendritic Cell Deficiency, Autosomal Recessive
|
|
|
| Dendritic Cell Deficiency |
|
|
| Esophageal Atresia |
|
Tracheoesophageal Fistula
|
Congenital Atresia Of Esophagus
|
|
Congenital Imperforate Esophagus
|
Imperforate Esophagus
|
|
Oesophageal Atresia
|
Te Fistula
|
|
Tef
|
Tracheoesophageal Fistula With Or Without Esophageal Atresia
|
|
|
| Oral Candidiasis |
|
Thrush
|
Candidiasis Of Mouth
|
|
Oral Moniliasis
|
Thrush, Oral
|
|
Candidiasis, Oral
|
Oral Thrush
|
|
Candidiasis
|
Equine Thrush
|
|
|
| Monocyte, Dendritic Cell, And Nk Cell Deficiency |
|
|
| Leukemia, Chronic Myeloid |
|
Chronic Myeloid Leukemia
|
Chronic Myelogenous Leukemia
|
|
CML
|
Chronic Granulocytic Leukemia
|
|
Leukemia, Philadelphia Chromosome-Positive, Resistant To Imatinib
|
Chronic Myeloid Leukaemia
|
|
Chronic Granulocytic Leukaemia
|
Chronic Myelogenous Leukaemia
|
|
Myeloid Leukemia, Chronic
|
Leukemia, Chronic Myelogenous
|
|
Leukemia, Chronic Myeloid, Philadelphia Chromosome Positive, Somatic
|
Cml - Chronic Myelogenous Leukemia
|
|
Cgl
|
Chronic Myelocytic Leukemia
|
|
Leukemia, Chronic Myeloid, Atypical
|
ACML
|
|
Atypical Chronic Myeloid Leukemia Bcr-Abl1 Negative
|
Myeloid Leukemia Chronic
|
|
Leukemia, Myeloid, Chronic
|
Leukemia, Myeloid, Chronic, Atypical, Bcr-Abl Negative
|
|
Cml- [Chronic Myeloid Leukaemia]
|
Cgl - [Chronic Granulocytic Leukaemia]
|
|
Chronic Myelocytic Leukaemia
|
|
|
| Immunodeficiency 21 |
|
Monocytopenia And Mycobacterial Infection Syndrome
|
Monomac
|
|
Gata2 Deficiency
|
Monocytopenia With Susceptibility To Infections
|
|
Dcml
|
IMD21
|
|
Dendritic Cell, Monocyte, B Lymphocyte, And Natural Killer Lymphocyte Deficiency
|
Monocytopenia With Susceptibility To Mycobacterial, Fungal, And Papillomavirus Infections And Myelodysplasia
|
|
Combined Immunodeficiency With Susceptibility To Mycobacterial, Viral, And Fungal Infections
|
Combined Immunodeficiency With Susceptibility To Mycobacterial, Viral And Fungal Infections
|
|
Dendritic Cell, Monocyte, B And Nk Lymphoid Deficiency
|
Monocyte-B-Natural Killer-Dendritic Cell Deficiency Syndrome
|
|
Monocytopenia With Mycobacterial, Fungal, And Papillomavirus Infections And Myelodysplasia
|
Combined Immunodeficiency With Mycobacterial, Viral, And Fungal Infections
|
|
Monocyte - B - Natural Killer - Dendritic Cell Deficiency
|
Combined Immunodeficiency With Susceptibility To Mycobacterial Viral And Fungal Infections
|
|
Dendritic Cell Monocyte Lymphocyte B And Natural Killer Lymphocyte Deficiency
|
Monocytopenia With Susceptibility To Mycobacterial Fungal And Papillomavirus Infections And Myelodysplasia
|
|
|
| Agammaglobulinemia |
|
Hypogammaglobulinemia
|
Ighm
|
|
Mu Heavy Chain Deficiency
|
Mu-Heavy Chain Disease
|
|
Mu-Hcd
|
Mu-Chain Disease
|
|
|
| Myeloproliferative Neoplasm |
|
Myeloproliferative Disorder
|
Chronic Myeloproliferative Disease
|
|
Myeloproliferative Neoplasms
|
Chronic Myeloproliferative Disorder
|
|
Cmpd
|
Cmpd, U
|
|
Chronic Myeloproliferative Disorders
|
Mpd
|
|
Mpn
|
Myeloproliferative Disorders
|
|
Myeloproliferative Disease
|
Campomelic Dysplasia
|
|
|
| Immunodeficiency 31b |
|
IMD31B
|
Immunodeficiency 31b, Mycobacterial And Viral Infections, Autosomal Recessive
|
|
Autosomal Recessive Stat1 Deficiency
|
Predisposition To Severe Viral Infection Due To Stat1 Deficiency
|
|
Susceptibility To Viral And Mycobacterial Infections Due To Stat1 Deficiency
|
Stat1 Deficiency, Autosomal Recessive
|
|
Autosomal Recessive Immunodeficiency 31b, Mycobacterial And Viral Infections
|
Stat1 Deficiency
|
|
Autosomal Recessive Susceptibility To Mycobacterial And Viral Infections
|
Mycobacterial And Viral Infections Due To Complete Stat1 Deficiency
|
|
Immunodeficiency, Type 31b, Mycobacterial And Viral Infections, Autosomal Recessive
|
|
|
| Axillary Adenitis |
|
|
| Tuberculous Salpingitis |
|
|
| Immunodeficiency 55 |
|
Combined Immunodeficiency Due To Gins1 Deficiency
|
IMD55
|
|
Cid Due To Gins1 Deficiency
|
Combined Immunodeficiency With Intrauterine Growth Retardation-Nk Cell Deficiency-Neutropenia
|
|
Combined Immunodeficiency With Intrauterine Growth Retardation-Natural Killer Cell Deficiency-Neutropenia
|
|
|
| Gastrointestinal Tularemia |
|
Enteric Tularemia
|
Intestinal Tularaemia
|
|
|
| Immunodeficiency 27b |
|
Autosomal Dominant Mendelian Susceptibility To Mycobacterial Diseases Due To Partial Ifngammar1 Deficiency
|
IMD27B
|
|
Immunodeficiency 27b, Mycobacteriosis, Autosomal Dominant
|
Ifngr1 Deficiency, Autosomal Dominant
|
|
Autosomal Dominant Mendelian Susceptibility To Mycobacterial Diseases Due To Partial Interferon Gamma Receptor 1 Deficiency
|
Autosomal Dominant Msmd Due To Partial Ifngammar1 Deficiency
|
|
Autosomal Dominant Msmd Due To Partial Interferon Gamma Receptor 1 Deficiency
|
Immunodeficiency 27b, Mycobacteriosis, Ad
|
|
Autosomal Dominant Ifngr1 Deficiency
|
Autosomal Dominant Immunodeficiency 27b, Mycobacteriosis
|
|
Immunodeficiency, Type 27b, Mycobacteriosis, Autosomal Dominant
|
|
|
| Systemic Lupus Erythematosus |
|
Lupus Nephritis
|
SLE
|
|
Disseminated Lupus Erythematosus
|
Systemic Lupus Erythematosus, Susceptibility To
|
|
Lupus Erythematosus, Systemic
|
Lupus Nephritis, Susceptibility To
|
|
Libman-Sacks Disease
|
Systemic Lupus Erythematosus Susceptibility To
|
|
Sle - Lupus Erythematosus, Systemic
|
Le Syndrome
|
|
Lupus
|
Lupus Erythematosus Systemic
|
|
Lupus Erythematosus, Systemic, Susceptibility To
|
Lupus Vulgaris
|
|
Lupus Erythematosus, Discoid
|
Lupus Erythematosus
|
|
Systemic Lupus Erythematosus Nos
|
Sle - [Systemic Lupus Erythematosus]
|
|
|
| Leukoencephalopathy, Hereditary Diffuse, With Spheroids 1 |
|
Hereditary Diffuse Leukoencephalopathy With Spheroids
|
Adult-Onset Leukoencephalopathy With Axonal Spheroids And Pigmented Glia
|
|
Alsp
|
Gpsc
|
|
Subcortical Gliosis Of Neumann
|
Leukoencephalopathy, Diffuse Hereditary, With Spheroids 1
|
|
Autosomal Dominant Leukoencephalopathy With Neuroaxonal Spheroids
|
Hdls
|
|
HDLS1
|
Leukoencephalopathy, Adult-Onset, With Axonal Spheroids And Pigmented Glia
|
|
Gliosis, Familial Progressive Subcortical
|
Leukoencephalopathy, Diffuse Hereditary, With Spheroids
|
|
Pold
|
Pigmentary Orthochromatic Leukodystrophy
|
|
Hereditary Diffuse Leukoencephalopathy With Axonal Spheroids And Pigmented Glia
|
Familial Progressive Subcortical Gliosis
|
|
Leukoencephalopathy With Neuroaxonal Spheroids, Autosomal Dominant
|
Dementia, Familial, Neumann Type
|
|
Adult-Onset Leukodystrophy With Neuroaxonal Spheroids
|
Hereditary Diffuse Leukoencephalopathy With Axonal Spheroids
|
|
Neuroaxonal Leukodystrophy
|
Fpsg
|
|
Familial Dementia, Neumann Type
|
Familial Dementia Neumann Type
|
|
Leukoencephalopathy, Diffuse Hereditary, With Spheroid
|
|
|
| Pitt-Hopkins Syndrome |
|
PTHS
|
Encephalopathy, Severe Epileptic, With Autonomic Dysfunction
|
|
Mental Retardation, Syndromal, With Intermittent Hyperventilation
|
Intellectual Disability, Wide Mouth, Distinctive Facial Features, And Intermittent Hyperventilation Followed By Apnea
|
|
Pitt Hopkins Syndrome
|
Phs
|
|
Encephalopathy Severe Epileptic With Autonomic Dysfunction
|
|
|
| Immune Deficiency Disease |
|
Immunodeficiency
|
Primary Immunodeficiency
|
|
Primary Immunodeficiency Disease
|
Immunologic Deficiency Syndromes
|
|
Hypoimmunity
|
Immune Deficiency Disorder
|
|
Immunodeficiency Syndrome
|
Immune Disorder
|
|
Primary Immune Deficiency Disorder
|
Immune System Diseases
|
|
Human Immunodeficiency Virus Infection
|
Hiv - [Human Immunodeficiency Virus Infection]
|
|
Hiv Positive Nos
|
Hiv Disease
|
|
Acquired Immune Deficiency Syndrome-Related Complex
|
Aids-Like Syndrome
|
|
Aids-Related Complex Nos
|
Arc - [Aids-Related Complex]
|
|
Immunodeficiency Due To Human Immunodeficiency Virus Infection
|
Unspecified Human Immunodeficiency Virus Disease
|
|
Hiv Disease Nos
|
Human Immunodeficiency Virus Positive Nos
|
|
Hiv Nos
|
Deficiency Of Complement Initial Pathway
|
|
Deficiency Of Complement Terminal Pathway
|
Cfdd - [Complement Factor D Deficiency]
|
|
Immunodeficiency With Nk-Cell - [Natural-Killer Cell] Deficiency
|
Nonfamilial Hypogammaglobulinaemia
|
|
Common Variable Immune Deficiency
|
Nonfamilial Agammaglobulinaemia
|
|
Common Variable Agammaglobulinaemia
|
Agammaglobulinaemia Nos
|
|
Agammaglobulinaemia Antibody Deficiency Syndrome
|
Hypogammaglobulinaemia Antibody Deficiency Syndrome
|
|
Acquired Agammaglobulinaemia Nos
|
Hypogammaglobulinaemia Nos
|
|
Hyper Igm
|
|
|
| Fanconi Anemia, Complementation Group A |
|
Fanconi Anemia
|
Fanconi Pancytopenia
|
|
Fanconi Anemia Complementation Group A
|
FANCA
|
|
Fa
|
Fanconi Panmyelopathy
|
|
Fanconi'S Anemia
|
Fanconi Anaemia
|
|
Fanconi'S Anaemia
|
Fanconi Hypoplastic Anemia
|
|
Estren-Dameshek Variant Of Fanconi Anemia
|
Estren-Dameshek Variant Of Fanconi Pancytopenia
|
|
Fanconi Anemia Estren-Dameshek Variant
|
Fanconis Anemia
|
|
|
| Behcet Syndrome |
|
Behcet Disease
|
Behcet'S Syndrome
|
|
Behcet'S Disease
|
Behçet Disease
|
|
Bd
|
Adamantiades-Behcet Disease
|
|
Triple Symptom Complex
|
Behçet'S Disease
|
|
Behet'S Syndrome
|
Bd Syndrome
|
|
Behçet Syndrome
|
Behçet'S Syndrome
|
|
Behcet Triple Symptom Complex
|
Malignant Aphthosis
|
|
Old Silk Route Disease
|
Adamantiades-Behçet Disease
|
|
|
| Leukemia, Acute Myeloid |
|
Acute Myeloid Leukemia
|
Leukemia, Acute Myelogenous
|
|
Acute Myelogenous Leukemia
|
AML
|
|
Leukemia, Acute Myeloid, Susceptibility To
|
Acute Myeloblastic Leukemia
|
|
Leukemia, Acute Myeloid, Reduced Survival In, Somatic
|
Acute Myeloid Leukaemia
|
|
Leukemia, Myelocytic, Acute
|
Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome
|
|
Secondary Aml
|
Acute Myelocytic Leukemia
|
|
Acute Myeloid Leukemia, Somatic
|
Leukemia, Acute Myeloid, Somatic
|
|
Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic
|
Acute Myeloblastic Leukaemia
|
|
Acute Myelogenous Leukaemia
|
Aml - Acute Myeloid Leukemia
|
|
Acute Myeloid Leukemia With Cebpa Somatic Mutations
|
Aml With Cebpa Somatic Mutations
|
|
Inherited Acute Myeloid Leukemia
|
Familial Aml
|
|
Inherited Aml
|
Pure Familial Aml
|
|
Pure Familial Acute Myeloid Leukemia
|
Secondary Acute Myeloid Leukemia
|
|
Therapy-Related Aml And Myelodysplastic Syndrome
|
Acute Myeloid Leukemia, Secondary
|
|
Acute Non-Lymphoblastic Leukemia
|
Acute Non-Lymphocytic Leukemia
|
|
Acute Biphenotypic Leukemia
|
Acute Undifferentiated Leukemia
|
|
Acute Myeloblastic Leukaemia With Multilineage Dysplasia
|
Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission
|
|
Acute Myeloid Leukaemia With Myelodysplasia-Related Features
|
|
|
