Search results for magt1

77 hits were found for magt1

# Family MCID Name MIFTS Score
1
IMM026 Immunodeficiency, X-Linked, with Magnesium Defect, Epstein-Barr Virus Infection, and Neoplasia 46 70.208
2
CNG607 Congenital Disorder of Glycosylation, Type Icc 17 31.121
3
c CNG411 Congenital Disorder of Glycosylation, Type in 66 22.852
4
LYM027 Lymphopenia 56 12.617
5
CMB007 Combined Immunodeficiency 56 11.116
6
DYS016 Dysgammaglobulinemia 33 8.854
7
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 7.982
8
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 64 7.694
9
IMM078 Immunodeficiency 21 57 7.694
10
CRN011 Coronin-1a Deficiency 19 7.694
11
c ATS204 Autosomal Recessive Non-Syndromic Intellectual Disability 47 7.694
12
IMM070 Immunodeficiency 13 39 7.694
13
c LYM107 Lymphoproliferative Syndrome 2 48 7.694
14
c ATM083 Autoimmune Lymphoproliferative Syndrome, Type Iii 37 7.694
15
SLC007 Selective Immunoglobulin Deficiency Disease 21 7.694
16
OMN001 Omenn Syndrome 63 7.694
17
IMM167 Immune Deficiency Disease 77 1.911
18
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.640
19
GLM045 Glioma 62 1.584
20
GLL048 Glial Tumor 52 1.584
21
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 1.339
22
P CLR023 Colorectal Cancer 100 1.286
23
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 1.228
24
P BCL017 B-Cell Lymphoma 57 1.159
25
P NRB001 Neuroblastoma 66 1.120
26
P HPT023 Hepatocellular Carcinoma 95 1.076
27
c MGR028 Migraine with or Without Aura 1 64 1.023
28
P ATS364 Autism 72 0.811
29
KPS004 Kaposi Sarcoma 76 0.788
30
SRC014 Sarcoma 64 0.788
31
SPN035 Spindle Cell Sarcoma 51 0.788
32
P BRS047 Breast Cancer 97 0.573
33
ALC007 Alcohol Dependence 65 0.573
34
P DNG005 Dengue Virus 55 0.552
35
P LYM118 Lymphoma 69 0.407
36
P HMP002 Hemophagocytic Lymphohistiocytosis 60 0.372
37
P HML002 Hemolytic Anemia 62 0.372
38
P THR014 Thrombocytopenia 66 0.372
39
OTT002 Otitis Media 71 0.333
40
CD4008 Cd4/cd8 T-Cell Ratio 19 0.333
41
P LYM033 Lymphoproliferative Syndrome 59 0.288
42
LSS003 Lassa Fever 49 0.288
43
MLL001 Molluscum Contagiosum 48 0.288
44
BCT022 Bacterial Infectious Disease 56 0.235
45
c HMP023 Hemophagocytic Lymphohistiocytosis, Familial, 5 42 0.235
46
SVR004 Severe Combined Immunodeficiency 71 0.235
47
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 65 0.235
48
P VSC011 Vasculitis 61 0.235
49
VRS001 Virus Associated Hemophagocytic Syndrome 27 0.235
50
LYM051 Lymphomatoid Granulomatosis 44 0.235
51
HMP028 Hemophagocytic Syndrome Associated with an Infection 24 0.235
52
c ANM038 Anemia, Autoimmune Hemolytic 63 0.166
53
P PLM037 Pulmonary Hypertension 69 0.166
54
IMM193 Immunodeficiency 58 27 0.166
56
c PRC016 Pre-Eclampsia 64 0.166
57
P OVR042 Ovarian Cancer 88 0.166
58
OVR105 Ovarian Serous Carcinoma 37 0.166
59
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.166
60
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 0.166
61
P APL001 Aplastic Anemia 73 0.166
62
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.166
63
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 0.166
64
PFF001 Pfeiffer Syndrome 77 0.166
65
P ANG001 Angelman Syndrome 65 0.166
66
IMM055 Immunodeficiency, Common Variable, 8, with Autoimmunity 43 0.166
67
c MNT196 Mental Retardation, X-Linked 92 18 0.166
68
RLN001 Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked 23 0.166
69
TCL003 T Cell Deficiency 44 0.166
70
PPL022 Papilloma 53 0.166
71
SQM002 Squamous Cell Papilloma 45 0.166
72
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.166
73
CMM004 Common Variable Immunodeficiency 72 0.166
74
ANX004 Anoxia 40 0.166
75
EVN001 Evans' Syndrome 46 0.166
76
PLY012 Polyhydramnios 46 0.166
77
ADN001 Adenosine Deaminase Deficiency 59 0.166
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