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"

173 hits were found for 'immunodeficiency with hyper igm'

# Family MCID Name MIFTS Score
1
IMM109 Immunodeficiency with Hyper Igm, Type 5 27 10.594
2
IMM111 Immunodeficiency, X-Linked, with Hyper-Igm 55 9.817
3
IMM105 Immunodeficiency with Hyper-Igm, Type 3 45 9.660
4
IMM104 Immunodeficiency with Hyper-Igm, Type 2 32 9.352
5
CD4003 Cd40 Ligand Deficiency 47 8.781
6
IMM131 Immunodeficiency with Hyper-Igm, Type 4 20 7.274
7
ECT076 Ectodermal Dysplasia, Hypohidrotic, with Immune Deficiency 25 5.022
8
P LYM118 Lymphoma 70 0.469
9
P LKM002 Leukemia 70 0.396
10
P HPT021 Hepatitis 70 0.380
11
CMM004 Common Variable Immunodeficiency 67 0.316
12
HV1006 Hiv-1 82 0.298
13
SVR004 Severe Combined Immunodeficiency 68 0.292
14
P ART022 Arthritis 75 0.280
15
PRM097 Primary Immunodeficiency Disease 61 0.262
16
P PNM007 Pneumonia 66 0.232
17
P BCL006 B-Cell Lymphomas 64 0.218
18
NTR005 Nutritional Deficiency Disease 39 0.217
19
P LPS004 Lupus Erythematosus 63 0.214
20
SRC014 Sarcoma 66 0.200
21
P THY032 Thyroiditis 54 0.199
22
CRB009 Cerebritis 38 0.199
23
c SYS001 Systemic Lupus Erythematosus 87 0.199
24
CHL071 Child Syndrome 58 0.198
25
TBR010 Tuberculosis 69 0.194
26
KDS001 Kid Syndrome 53 0.192
27
P ADN016 Adenocarcinoma 69 0.192
28
c CHR090 Chronic Lymphocytic Leukemia 74 0.190
29
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.189
30
PRS047 Prostatitis 56 0.187
31
P LVR013 Liver Disease 72 0.184
32
LYM019 Lymphosarcoma 53 0.183
33
P PRS040 Prostate Cancer 89 0.183
34
HMT018 Hematopoietic Stem Cell Transplantation 41 0.182
35
c HPT016 Hepatitis B 64 0.182
36
END072 Endotheliitis 42 0.181
37
P GLM007 Glomerulonephritis 56 0.179
38
P NRV006 Nervous System Cancer 62 0.178
39
P ENC004 Encephalitis 61 0.174
40
P ATX004 Ataxia 53 0.171
41
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.169
42
P NTR004 Neutropenia 59 0.168
43
BLD054 Blood Protein Disease 40 0.168
44
P OBS005 Obesity 93 0.167
45
P AMY004 Amyloidosis 64 0.164
46
DRM006 Dermatitis 61 0.163
47
IPX001 Ipex Syndrome 45 0.162
48
P HML002 Hemolytic Anemia 60 0.162
49
HPT023 Hepatocellular Carcinoma 91 0.161
50
P MYP004 Myopathy 67 0.156
51
P CLR023 Colorectal Cancer 97 0.154
52
P ESP024 Esophagitis 62 0.150
53
P MNN013 Meningitis 65 0.149
54
SKN016 Skin Disease 68 0.149
55
ALL026 Allergic Hypersensitivity Disease 53 0.148
56
P CRV039 Cervicitis 44 0.147
57
ADL002 Adult Syndrome 53 0.146
58
GST053 Gastric Cancer 77 0.146
59
ACD009 Acid-Labile Subunit, Deficiency of 48 0.145
60
P CND004 Candidiasis 57 0.143
61
P ESN007 Eosinophilia 61 0.143
62
P RBL001 Rubella 56 0.143
63
LYM040 Lymphoblastic Lymphoma 54 0.143
64
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.143
65
P MYC007 Myocardial Infarction 79 0.142
66
ALR002 Al-Raqad Syndrome 36 0.140
67
P DRR001 Diarrhea 51 0.139
68
P HYP086 Hypothyroidism 65 0.139
69
P NRV007 Nervous System Disease 71 0.139
70
P TCL004 T-Cell Leukemia 46 0.138
71
LNG099 Lung Disease 62 0.138
72
c ATM010 Autoimmune Hemolytic Anemia 60 0.137
73
DFF005 Diffuse Large B-Cell Lymphoma 56 0.137
74
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.132
75
P INF038 Influenza 74 0.132
76
P HRP006 Herpes Simplex 65 0.130
77
c CNT035 Central Nervous System Disease 59 0.130
78
SPL018 Splenomegaly 44 0.129
79
CNN005 Connective Tissue Disease 61 0.129
80
P ATX030 Ataxia-Telangiectasia 76 0.128
81
TCL003 T Cell Deficiency 45 0.127
82
RSP006 Respiratory System Disease 62 0.126
83
P AGM001 Agammaglobulinemia 64 0.125
84
VND001 Vein Disease 52 0.123
85
MNT001 Mantle Cell Lymphoma 70 0.123
86
NRM005 Neuromuscular Disease 57 0.122
87
CYT008 Cytomegalovirus Infection 51 0.122
88
HDG012 Hodgkin Lymphoma 73 0.121
89
ATH003 Atherosclerosis 62 0.117
90
MLR004 Malaria 79 0.116
91
WTH001 Withdrawal Disorder 41 0.116
92
PRG009 Progressive Multifocal Leukoencephalopathy 50 0.116
93
IMM025 Immunoglobulin a Deficiency 2 27 0.115
94
c HPT015 Hepatitis D 52 0.114
95
NRN004 Neuroendocrine Tumor 54 0.114
96
MTH009 Mouth Disease 63 0.113
97
VSC007 Vascular Disease 67 0.110
98
P PRP019 Peripheral Nervous System Disease 54 0.110
99
BRK010 Burkitt Lymphoma 66 0.109
100
MGL016 Megaloblastic Anemia-1, Finnish Type 46 0.109
101
P CTR002 Cataract 57 0.109
102
MSC004 Muscle Tissue Disease 36 0.108
103
P LPR003 Leprosy 68 0.108
104
ECT006 Ectodermal Dysplasia 47 0.107
105
c INH020 Inherited Metabolic Disorder 49 0.103
106
CRH001 Crohn's Disease 76 0.103
107
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.103
108
HST011 Histoplasmosis 54 0.102
109
P CHL066 Cholangitis 49 0.102
110
DYS016 Dysgammaglobulinemia 37 0.101
111
BCL002 B Cell Deficiency 50 0.099
112
P NRB001 Neuroblastoma 69 0.098
113
IMM077 Immunodeficiency 20 29 0.097
114
HPT074 Hepatic Adenoma, Somatic 51 0.096
115
P EXN002 Exanthem 57 0.095
116
IMM044 Immunoglobulin G Deficiency 35 0.095
117
P MYS003 Myasthenia Gravis 65 0.095
118
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.094
119
HNM002 Hinman Syndrome 25 0.093
120
P SCL009 Sclerosing Cholangitis 47 0.093
121
P GRV001 Graves' Disease 61 0.093
122
TTN003 Tetanus 61 0.092
123
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.091
124
MNN009 Meningoencephalitis 45 0.091
125
BRN022 Bronchiectasis 47 0.090
126
P XLN007 X-Linked Disease 34 0.089
127
IMN002 Iminoglycinuria, Digenic 33 0.088
128
BRN002 Bronchiolitis 56 0.087
129
IMM085 Immunodeficiency 25 25 0.087
130
HDC001 Headache 54 0.087
131
P END033 Endocarditis 52 0.086
132
IMM120 Immunodeficiency 40 26 0.084
133
THR013 Thoracic Outlet Syndrome 49 0.083
134
OTT002 Otitis Media 66 0.082
135
OMN001 Omenn Syndrome 61 0.082
136
URT039 Urticaria 59 0.082
137
GRN017 Granulocytopenia 42 0.081
138
ACT049 Acute Disseminated Encephalomyelitis 49 0.081
139
PRC002 Paracoccidioidomycosis 55 0.080
140
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.080
141
THR004 Thrombocytosis 55 0.079
142
LYM021 Lymphadenitis 58 0.079
143
FCT003 Factor X Deficiency 62 0.079
144
PRT037 Pertussis 64 0.077
145
P PLM006 Pulmonary Alveolar Proteinosis 48 0.076
146
LPT001 Leptospirosis 63 0.076
147
PNM001 Pneumocystosis 50 0.074
148
P CSH001 Cushing's Syndrome 64 0.074
149
P PLY018 Polycythemia 57 0.074
150
P PNV001 Panuveitis 49 0.071
151
HYP627 Hyper-Igm Syndrome with Susceptibility to Opportunistic Infections 4 0.071
152
HYP067 Hyperimmunoglobulin Syndrome 29 0.071
153
CMB023 Combined Immunodeficiency, X-Linked, Moderate 51 0.071
154
CRN017 Coronary Thrombosis 48 0.070
155
HYP626 Hyper-Igm Syndrome Without Susceptibility to Opportunistic Infections 4 0.070
156
CHL014 Cholera 55 0.069
157
CHR063 Chronic Mucocutaneous Candidiasis 61 0.068
158
LYS002 Lysosomal Storage Disease 52 0.065
159
VNW001 Von Willebrand's Disease 61 0.065
160
CRS001 Crescentic Glomerulonephritis 41 0.064
161
LRG008 Large Granular Lymphocyte Leukemia 38 0.061
162
EVN001 Evans' Syndrome 43 0.061
163
ADP007 Adie Pupil 34 0.059
164
DSC009 Discoid Lupus Erythematosus 44 0.057
165
PRL032 Perlman Syndrome 55 0.057
166
LPR001 Lepromatous Leprosy 49 0.056
167
c SVR003 Severe Congenital Neutropenia 56 0.056
168
RCH001 Richter's Syndrome 44 0.051
169
KTL001 Keutel Syndrome 35 0.044
170
c JVN024 Juvenile Hereditary Hemochromatosis 28 0.042
171
P SMP007 Simpson-Golabi-Behmel Syndrome, Type 1 48 0.042
172
c MLG036 Malignant Spiradenoma 33 0.040
173
c PST057 Postaxial Polydactyly, Type A2 20 0.039