Search results for "immunodeficiency with hyper igm"

The MalaCard for "immunodeficiency with hyper igm" has been retired.
Searching MalaCards for entries containing "immunodeficiency with hyper igm"

165 hits were found for 'immunodeficiency with hyper igm'

# Family MCID Name MIFTS Score
1
IMM111 Immunodeficiency, X-Linked, with Hyper-Igm 55 9.737
2
IMM109 Immunodeficiency with Hyper Igm, Type 5 26 9.509
3
IMM104 Immunodeficiency with Hyper-Igm, Type 2 31 8.661
4
CD4003 Cd40 Ligand Deficiency 47 8.097
5
IMM105 Immunodeficiency with Hyper-Igm, Type 3 23 7.558
6
IMM131 Immunodeficiency with Hyper-Igm, Type 4 17 6.401
7
CD4002 Cd40 Deficiency 38 5.485
8
ECT076 Ectodermal Dysplasia, Hypohidrotic, with Immune Deficiency 26 4.269
9
P LYM118 Lymphoma 68 0.472
10
P LKM002 Leukemia 70 0.397
11
P HPT021 Hepatitis 74 0.379
12
CMM004 Common Variable Immunodeficiency 68 0.314
13
SVR004 Severe Combined Immunodeficiency 71 0.299
14
P ART022 Arthritis 73 0.287
15
HV1006 Hiv-1 80 0.269
16
P PNM007 Pneumonia 67 0.248
17
IMM102 Immunodeficiency 14 33 0.237
18
P BCL006 B-Cell Lymphomas 64 0.226
19
IPX001 Ipex Syndrome 35 0.224
20
P LPS004 Lupus Erythematosus 63 0.219
21
NTR005 Nutritional Deficiency Disease 51 0.216
22
c SYS001 Systemic Lupus Erythematosus 87 0.204
23
CRB009 Cerebritis 36 0.204
24
P THY032 Thyroiditis 57 0.201
25
SRC014 Sarcoma 66 0.200
26
TBR010 Tuberculosis 70 0.197
27
P ADN016 Adenocarcinoma 69 0.193
28
c CHR090 Chronic Lymphocytic Leukemia 73 0.191
29
P LVR013 Liver Disease 76 0.191
30
PRS047 Prostatitis 56 0.189
31
ALR002 Al-Raqad Syndrome 36 0.188
32
P GLM007 Glomerulonephritis 56 0.187
33
LYM019 Lymphosarcoma 52 0.185
34
HMT018 Hematopoietic Stem Cell Transplantation 39 0.184
35
P PRS040 Prostate Cancer 89 0.183
36
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.182
37
c HPT016 Hepatitis B 61 0.182
38
END072 Endotheliitis 41 0.182
39
KDS001 Kid Syndrome 53 0.180
40
CHL071 Child Syndrome 58 0.180
41
P NTR004 Neutropenia 59 0.178
42
C3D001 C3 Deficiency 50 0.177
43
P ENC004 Encephalitis 60 0.176
44
P NRV006 Nervous System Cancer 62 0.173
45
P OBS005 Obesity 91 0.172
46
P ATX004 Ataxia 53 0.172
47
DRM006 Dermatitis 58 0.167
48
P HML002 Hemolytic Anemia 60 0.167
49
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.166
50
P AMY004 Amyloidosis 63 0.166
51
ADL002 Adult Syndrome 53 0.165
52
BLD054 Blood Protein Disease 38 0.165
53
HPT023 Hepatocellular Carcinoma 90 0.163
54
P DRR001 Diarrhea 60 0.161
55
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.157
56
P MNN013 Meningitis 66 0.154
57
P CRV039 Cervicitis 45 0.153
58
P MYP004 Myopathy 67 0.153
59
P ESP024 Esophagitis 62 0.151
60
P ESN007 Eosinophilia 61 0.151
61
SKN016 Skin Disease 69 0.151
62
GST053 Gastric Cancer 52 0.149
63
P NRV007 Nervous System Disease 71 0.146
64
P CND004 Candidiasis 58 0.146
65
P HYP086 Hypothyroidism 63 0.144
66
ALL026 Allergic Hypersensitivity Disease 53 0.144
67
P RBL001 Rubella 54 0.144
68
ACD009 Acid-Labile Subunit, Deficiency of 37 0.144
69
LYM040 Lymphoblastic Lymphoma 51 0.143
70
P MYC007 Myocardial Infarction 80 0.143
71
c ATM010 Autoimmune Hemolytic Anemia 59 0.142
72
P INF038 Influenza 71 0.141
73
DFF005 Diffuse Large B-Cell Lymphoma 57 0.141
74
LNG099 Lung Disease 63 0.140
75
P TCL004 T-Cell Leukemia 44 0.139
76
P HRP006 Herpes Simplex 65 0.138
77
c CNT035 Central Nervous System Disease 60 0.134
78
TCL003 T Cell Deficiency 44 0.132
79
CNN005 Connective Tissue Disease 60 0.131
80
SPL018 Splenomegaly 45 0.129
81
P ATX030 Ataxia-Telangiectasia 78 0.129
82
P AGM001 Agammaglobulinemia 63 0.129
83
HDG012 Hodgkin Lymphoma 75 0.128
84
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.126
85
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.126
86
MNT001 Mantle Cell Lymphoma 72 0.125
87
CYT008 Cytomegalovirus Infection 51 0.124
88
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.122
89
NRM005 Neuromuscular Disease 56 0.121
90
ATH003 Atherosclerosis 63 0.119
91
MLR004 Malaria 80 0.119
92
NRN004 Neuroendocrine Tumor 54 0.116
93
HST011 Histoplasmosis 54 0.116
94
c HPT015 Hepatitis D 51 0.115
95
P CTR002 Cataract 57 0.114
96
WTH001 Withdrawal Disorder 36 0.114
97
THR013 Thoracic Outlet Syndrome 48 0.114
98
BRK010 Burkitt Lymphoma 66 0.113
99
IMM025 Immunoglobulin a Deficiency 2 27 0.111
100
P LPR003 Leprosy 70 0.111
101
ECT006 Ectodermal Dysplasia 46 0.110
102
IMN002 Iminoglycinuria, Digenic 35 0.110
103
VSC007 Vascular Disease 51 0.109
104
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.109
105
P CHL066 Cholangitis 48 0.107
106
DYS016 Dysgammaglobulinemia 37 0.105
107
c INH020 Inherited Metabolic Disorder 49 0.104
108
CRH001 Crohn's Disease 76 0.102
109
IMM044 Immunoglobulin G Deficiency 22 0.101
110
P NRB001 Neuroblastoma 70 0.099
111
BCL002 B Cell Deficiency 50 0.099
112
IMM077 Immunodeficiency 20 28 0.098
113
P GRV001 Graves' Disease 62 0.097
114
P SCL009 Sclerosing Cholangitis 47 0.097
115
P EXN002 Exanthem 57 0.097
116
TTN003 Tetanus 62 0.097
117
P MYS003 Myasthenia Gravis 64 0.096
118
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.096
119
P END033 Endocarditis 52 0.095
120
MGL001 Megaloblastic Anemia 51 0.095
121
ACT049 Acute Disseminated Encephalomyelitis 50 0.094
122
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.093
123
BRN022 Bronchiectasis 55 0.093
124
MNN009 Meningoencephalitis 42 0.092
125
P XLN007 X-Linked Disease 34 0.090
126
HDC001 Headache 52 0.088
127
P CSH001 Cushing's Syndrome 65 0.088
128
IMM085 Immunodeficiency 25 25 0.087
129
IMM120 Immunodeficiency 40 24 0.084
130
OMN001 Omenn Syndrome 61 0.082
131
URT039 Urticaria 58 0.082
132
P PLM006 Pulmonary Alveolar Proteinosis 46 0.081
133
PRC002 Paracoccidioidomycosis 57 0.081
134
GRN017 Granulocytopenia 39 0.081
135
P PNV001 Panuveitis 50 0.080
136
LYM021 Lymphadenitis 58 0.079
137
THR004 Thrombocytosis 55 0.079
138
FCT003 Factor X Deficiency 62 0.079
139
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 40 0.078
140
OTP003 Oto-Palatal-Digital Syndrome 14 0.077
141
LPT001 Leptospirosis 65 0.076
142
PRT037 Pertussis 63 0.076
143
P PLY018 Polycythemia 58 0.073
144
CHR063 Chronic Mucocutaneous Candidiasis 61 0.073
145
PRL032 Perlman Syndrome 55 0.073
146
HYP627 Hyper-Igm Syndrome with Susceptibility to Opportunistic Infections 4 0.072
147
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.071
148
HYP626 Hyper-Igm Syndrome Without Susceptibility to Opportunistic Infections 4 0.070
149
CRN017 Coronary Thrombosis 46 0.070
150
CRS001 Crescentic Glomerulonephritis 41 0.069
151
CHL014 Cholera 56 0.069
152
LYS002 Lysosomal Storage Disease 51 0.067
153
EVN001 Evans' Syndrome 39 0.065
154
ADR013 Adrenal Gland Hyperfunction 47 0.064
155
P SMP003 Simpson-Golabi-Behmel Syndrome 46 0.064
156
LRG008 Large Granular Lymphocyte Leukemia 39 0.064
157
TRC008 Trachoma 50 0.061
158
KTL001 Keutel Syndrome 37 0.060
159
DSC009 Discoid Lupus Erythematosus 40 0.058
160
c SMP007 Simpson-Golabi-Behmel Syndrome, Type 1 38 0.057
161
LPR001 Lepromatous Leprosy 50 0.056
162
c MLG036 Malignant Spiradenoma 33 0.056
163
c PST057 Postaxial Polydactyly, Type A2 21 0.056
164
c SVR003 Severe Congenital Neutropenia 54 0.056
165
RCH001 Richter's Syndrome 45 0.051