Search results for immunodeficiency with hyper igm

180 hits were found for immunodeficiency with hyper igm

# Family MCID Name MIFTS Score
1
IMM109 Immunodeficiency with Hyper Igm, Type 5 27 10.523
2
IMM111 Immunodeficiency, X-Linked, with Hyper-Igm 54 9.750
3
IMM104 Immunodeficiency with Hyper-Igm, Type 2 47 9.632
4
IMM105 Immunodeficiency with Hyper-Igm, Type 3 45 9.593
5
CD4003 Cd40 Ligand Deficiency 46 8.725
6
IMM131 Immunodeficiency with Hyper-Igm, Type 4 37 7.662
7
ECT076 Ectodermal Dysplasia, Hypohidrotic, with Immune Deficiency 25 4.984
8
P LYM118 Lymphoma 69 0.449
9
P LKM002 Leukemia 71 0.384
10
P HPT021 Hepatitis 69 0.364
11
CMM004 Common Variable Immunodeficiency 68 0.290
12
P ART022 Arthritis 75 0.274
13
SVR004 Severe Combined Immunodeficiency 69 0.262
14
HV1006 Hiv-1 80 0.246
15
PRM097 Primary Immunodeficiency Disease 60 0.243
16
P PNM007 Pneumonia 68 0.228
17
P BCL006 B-Cell Lymphomas 65 0.214
18
P LPS004 Lupus Erythematosus 64 0.209
19
NTR005 Nutritional Deficiency Disease 36 0.204
20
c SYS001 Systemic Lupus Erythematosus 86 0.195
21
P THY032 Thyroiditis 54 0.193
22
CRB009 Cerebritis 39 0.191
23
SRC014 Sarcoma 66 0.191
24
P ADN016 Adenocarcinoma 69 0.189
25
c CHR090 Chronic Lymphocytic Leukemia 76 0.186
26
TBR010 Tuberculosis 70 0.182
27
PRS047 Prostatitis 56 0.182
28
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.180
29
P PRS040 Prostate Cancer 90 0.178
30
KDS001 Kid Syndrome 53 0.178
31
CHL071 Child Syndrome 58 0.178
32
P GLM007 Glomerulonephritis 59 0.176
33
P LVR013 Liver Disease 75 0.176
34
LYM019 Lymphosarcoma 53 0.175
35
c HPT016 Hepatitis B 64 0.174
36
HMT018 Hematopoietic Stem Cell Transplantation 41 0.173
37
END072 Endotheliitis 42 0.173
38
P ATX004 Ataxia 53 0.167
39
P ENC004 Encephalitis 63 0.166
40
P OBS005 Obesity 92 0.166
41
BLD054 Blood Protein Disease 37 0.165
42
P NTR004 Neutropenia 59 0.164
43
P AMY004 Amyloidosis 65 0.161
44
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.161
45
DRM006 Dermatitis 66 0.159
46
P HPT023 Hepatocellular Carcinoma 92 0.159
47
P HML002 Hemolytic Anemia 62 0.158
48
P CLR023 Colorectal Cancer 97 0.152
49
IPX001 Ipex Syndrome 45 0.152
50
SQM006 Squamous Cell Carcinoma 70 0.152
51
P MYP004 Myopathy 67 0.151
52
P NRV006 Nervous System Cancer 60 0.151
53
THR024 Thrombosis 57 0.146
54
GST053 Gastric Cancer 78 0.146
55
P ESP024 Esophagitis 61 0.145
56
P MYC007 Myocardial Infarction 79 0.144
57
SKN016 Skin Disease 66 0.144
58
ALL026 Allergic Hypersensitivity Disease 52 0.144
59
ADL002 Adult Syndrome 52 0.143
60
P MNN013 Meningitis 67 0.143
61
P CRV039 Cervicitis 45 0.143
62
ALR002 Al-Raqad Syndrome 36 0.142
63
P RBL001 Rubella 57 0.141
64
LNG099 Lung Disease 64 0.141
65
LYM040 Lymphoblastic Lymphoma 53 0.140
66
P HYP086 Hypothyroidism 64 0.138
67
ACD009 Acid-Labile Subunit, Deficiency of 45 0.137
68
P CND004 Candidiasis 57 0.136
69
c ATM010 Autoimmune Hemolytic Anemia 60 0.135
70
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.135
71
P DRR001 Diarrhea 60 0.134
72
P TCL004 T-Cell Leukemia 47 0.133
73
DFF005 Diffuse Large B-Cell Lymphoma 59 0.132
74
P INF038 Influenza 72 0.132
75
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.129
76
RSP006 Respiratory System Disease 58 0.129
77
P NRV007 Nervous System Disease 71 0.129
78
CNN005 Connective Tissue Disease 62 0.127
79
SPL018 Splenomegaly 44 0.127
80
MGL001 Megaloblastic Anemia 50 0.124
81
P ATX030 Ataxia-Telangiectasia 77 0.124
82
P HRP006 Herpes Simplex 65 0.123
83
MCS002 Mucositis 55 0.123
84
MNT001 Mantle Cell Lymphoma 72 0.121
85
ATH003 Atherosclerosis 65 0.119
86
CYT008 Cytomegalovirus Infection 52 0.119
87
ISC004 Ischemia 61 0.119
88
P AGM001 Agammaglobulinemia 64 0.119
89
TCL003 T Cell Deficiency 45 0.118
90
HDG012 Hodgkin Lymphoma 77 0.117
91
NRM005 Neuromuscular Disease 56 0.117
92
WTH001 Withdrawal Disorder 37 0.115
93
MLR004 Malaria 83 0.114
94
PRP019 Peripheral Nervous System Disease 55 0.113
95
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.112
96
c HPT015 Hepatitis D 52 0.111
97
IMM025 Immunoglobulin a Deficiency 2 24 0.111
98
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.111
99
VSC007 Vascular Disease 67 0.109
100
BRK010 Burkitt Lymphoma 69 0.108
101
MTH009 Mouth Disease 61 0.108
102
P CTR002 Cataract 58 0.108
103
P LPR003 Leprosy 69 0.108
104
MSC004 Muscle Tissue Disease 34 0.107
105
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.106
106
LPD008 Lipid Metabolism Disorder 58 0.103
107
CRH001 Crohn's Disease 75 0.101
108
c INH020 Inherited Metabolic Disorder 49 0.100
109
P CHL066 Cholangitis 42 0.099
110
ECT006 Ectodermal Dysplasia 52 0.099
111
HPT074 Hepatic Adenoma, Somatic 50 0.099
112
DYS016 Dysgammaglobulinemia 37 0.098
113
IMM044 Immunoglobulin G Deficiency 33 0.097
114
HNM002 Hinman Syndrome 25 0.097
115
HST011 Histoplasmosis 52 0.096
116
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.095
117
P MYS003 Myasthenia Gravis 67 0.094
118
P NRB001 Neuroblastoma 70 0.094
119
P EXN002 Exanthem 57 0.094
120
P SCL009 Sclerosing Cholangitis 48 0.093
121
BCL002 B Cell Deficiency 49 0.093
122
TTN003 Tetanus 61 0.092
123
P END033 Endocarditis 54 0.092
124
P GRV001 Graves' Disease 59 0.091
125
IMM077 Immunodeficiency 20 27 0.091
126
BRN002 Bronchiolitis 56 0.090
127
SFT003 Soft Tissue Sarcoma 57 0.090
128
GST045 Gastroenteritis 59 0.090
129
MNN009 Meningoencephalitis 47 0.089
130
GRW007 Growth Hormone Deficiency 50 0.087
131
HDC001 Headache 54 0.086
132
BRN022 Bronchiectasis 50 0.086
133
IMN002 Iminoglycinuria, Digenic 34 0.085
134
OTT002 Otitis Media 66 0.085
135
THR004 Thrombocytosis 55 0.085
136
P XLN007 X-Linked Disease 34 0.085
137
c ACT210 Acute Respiratory Distress Syndrome 57 0.084
138
CMB003 Combined T Cell and B Cell Immunodeficiency 42 0.083
139
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.082
140
IMM085 Immunodeficiency 25 23 0.081
141
OMN001 Omenn Syndrome 67 0.080
142
THR013 Thoracic Outlet Syndrome 50 0.080
143
LYM021 Lymphadenitis 58 0.080
144
LPT001 Leptospirosis 62 0.080
145
PRC002 Paracoccidioidomycosis 55 0.079
146
URT039 Urticaria 57 0.079
147
GRN017 Granulocytopenia 44 0.079
148
IMM120 Immunodeficiency 40 24 0.079
149
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.076
150
FCT003 Factor X Deficiency 61 0.076
151
PRT037 Pertussis 64 0.075
152
CRN017 Coronary Thrombosis 48 0.075
153
P PLM006 Pulmonary Alveolar Proteinosis 48 0.074
154
PNM001 Pneumocystosis 50 0.072
155
P PLY018 Polycythemia 58 0.072
156
HYP067 Hyperimmunoglobulin Syndrome 28 0.071
157
HYP627 Hyper-Igm Syndrome with Susceptibility to Opportunistic Infections 4 0.070
158
P ECL001 Eclampsia 54 0.070
159
CHR063 Chronic Mucocutaneous Candidiasis 63 0.070
160
VNW001 Von Willebrand's Disease 61 0.070
161
HYP626 Hyper-Igm Syndrome Without Susceptibility to Opportunistic Infections 4 0.068
162
CHL014 Cholera 53 0.066
163
P PNV001 Panuveitis 50 0.066
164
CRS001 Crescentic Glomerulonephritis 42 0.062
165
LYS002 Lysosomal Storage Disease 52 0.061
166
OBS001 Obstructive Jaundice 48 0.060
167
LRG008 Large Granular Lymphocyte Leukemia 39 0.059
168
LPR001 Lepromatous Leprosy 50 0.059
169
EVN001 Evans' Syndrome 43 0.058
170
DSC009 Discoid Lupus Erythematosus 45 0.056
171
PRL032 Perlman Syndrome 50 0.056
172
c SVR003 Severe Congenital Neutropenia 56 0.054
173
BDY001 Body Dysmorphic Disorder 39 0.053
174
P SMP003 Simpson-Golabi-Behmel Syndrome 51 0.047
175
c JVN024 Juvenile Hereditary Hemochromatosis 29 0.041
176
c SMP007 Simpson-Golabi-Behmel Syndrome, Type 1 40 0.040
177
CRN237 Corneal Dystrophy, Avellino Type 30 0.040
178
P OMD003 Omodysplasia 27 0.040
179
c SPS118 Spastic Paraplegia 36, Autosomal Dominant 25 0.038
180
c PST057 Postaxial Polydactyly, Type A2 21 0.038
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