Search results for ada2

176 hits were found for ada2

# Family MCID Name MIFTS Score
1
VSC058 Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome 49 89.581
2
SND002 Sneddon Syndrome 47 41.186
3
P PLY017 Polyarteritis Nodosa 60 21.869
4
P DMN001 Diamond-Blackfan Anemia 73 19.665
5
BHC003 Behcet Syndrome 71 19.110
6
SPL018 Splenomegaly 47 18.971
7
P VSC011 Vasculitis 61 18.796
8
CTY001 Cat Eye Syndrome 45 17.190
9
PLR008 Pleurisy 49 12.129
10
GRN037 Granulomatosis with Polyangiitis 67 11.681
11
CRB039 Cerebrovascular Disease 65 10.651
12
LVD003 Livedoid Vasculitis 35 8.589
13
STN011 Sting-Associated Vasculopathy with Onset in Infancy 44 7.675
14
P ACR001 Aicardi-Goutieres Syndrome 63 7.532
15
SDR009 Sideroblastic Anemia with B-Cell Immunodeficiency, Periodic Fevers, and Developmental Delay 44 7.532
16
KPS004 Kaposi Sarcoma 76 7.532
17
MNN002 Mononeuritis Multiplex 38 7.532
18
TST007 Testicular Infarct 21 7.532
19
EPD018 Epididymo-Orchitis 31 7.532
20
P NTR004 Neutropenia 62 2.553
21
P EXN002 Exanthem 58 2.473
22
CMB007 Combined Immunodeficiency 56 1.691
23
SVR004 Severe Combined Immunodeficiency 71 1.691
24
ATS010 Autosomal Recessive Disease 42 1.617
25
CND006 Candida Glabrata 29 1.551
26
P AGM001 Agammaglobulinemia 67 1.515
27
P PRR002 Pure Red-Cell Aplasia 46 1.464
28
P THR014 Thrombocytopenia 66 1.435
29
STR067 Stroke, Ischemic 79 1.377
30
ADN001 Adenosine Deaminase Deficiency 59 1.365
31
IMM167 Immune Deficiency Disease 77 1.338
32
P LYM033 Lymphoproliferative Syndrome 59 1.310
33
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 1.310
34
CTN019 Cutaneous Polyarteritis Nodosa 25 1.246
35
P MYL006 Myeloid Leukemia 60 1.196
36
P CND004 Candidiasis 57 1.132
37
c SYS066 Systemic Polyarteritis Nodosa 26 1.132
38
c SYS001 Systemic Lupus Erythematosus 86 1.109
39
LYM027 Lymphopenia 56 1.109
40
P LPS004 Lupus Erythematosus 61 1.109
41
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 1.058
42
ENT011 Enterocolitis 55 1.030
43
PLM001 Pulmonary Tuberculosis 69 1.030
44
MCR088 Microscopic Polyangiitis 51 1.030
45
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.999
46
ACT098 Acute Erythroid Leukemia 55 0.999
47
P BRS047 Breast Cancer 97 0.993
48
P NNN037 Noonan Syndrome-Like Disorder with Loose Anagen Hair 49 0.965
49
P NNN008 Noonan Syndrome 1 76 0.965
50
c PSD047 Pseudo-Turner Syndrome 52 0.965
51
EVN001 Evans' Syndrome 46 0.958
52
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.926
53
P LKM062 Leukemia, Acute Lymphoblastic 69 0.822
54
PRT251 Proteinuria, Chronic Benign 58 0.821
55
IMM003 Immunoglobulin Alpha Deficiency 44 0.821
56
LKC009 Leukocyte Adhesion Deficiency, Type I 70 0.821
57
P WSK001 Wiskott-Aldrich Syndrome 72 0.821
58
NPH003 Nephrocalcinosis 49 0.821
59
P CHR012 Chronic Granulomatous Disease 69 0.821
60
c MCR115 Microvascular Complications of Diabetes 5 65 0.732
61
c THY056 Thyroid Dyshormonogenesis 3 32 0.678
62
CST005 Castleman Disease 56 0.678
63
AMG001 Amegakaryocytic Thrombocytopenia, Congenital 55 0.678
64
P HMN032 Human Herpesvirus 8 47 0.678
65
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.678
66
MLT113 Multicentric Castleman Disease 47 0.678
67
PLY010 Polyclonal Hypergammaglobulinemia 35 0.678
68
PRP030 Purpura 54 0.678
69
UNC014 Unicentric Castleman Disease 22 0.678
70
PLR001 Pleural Tuberculosis 49 0.674
71
HYP066 Hyperglycemia 60 0.642
72
P PNC035 Pancreatic Cancer 86 0.573
73
RTN020 Retinal Vascular Disease 45 0.537
74
c JVN010 Juvenile Rheumatoid Arthritis 66 0.518
75
PRT036 Peritonitis 65 0.518
76
THR004 Thrombocytosis 52 0.498
77
HMN044 Human Immunodeficiency Virus Type 1 76 0.454
78
P LKM002 Leukemia 66 0.454
79
P ART022 Arthritis 70 0.454
80
KWS002 Kawasaki Disease 65 0.431
81
MCR225 Macrophage Activation Syndrome 45 0.431
82
P ADL017 Adult T-Cell Leukemia 54 0.406
83
P DRM010 Dermatomyositis 61 0.406
84
P MYC084 Mycobacterium Tuberculosis 1 68 0.406
85
CHL028 Childhood Type Dermatomyositis 58 0.406
86
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.406
87
TBR008 Tuberculous Peritonitis 35 0.406
88
47X002 47,xyy 48 0.406
89
c LKM005 Leukemia, T-Cell, Chronic 33 0.406
90
P RHM011 Rheumatoid Arthritis 81 0.380
91
MLR004 Malaria 78 0.380
92
CMM004 Common Variable Immunodeficiency 72 0.380
93
P LVR013 Liver Disease 68 0.380
94
ART140 Arteries, Anomalies of 52 0.352
95
LPP008 Lipoprotein Quantitative Trait Locus 65 0.352
96
c PRC016 Pre-Eclampsia 64 0.352
97
P MYS005 Myositis 56 0.352
98
c TYP008 Type 1 Diabetes Mellitus 77 0.352
99
PFF001 Pfeiffer Syndrome 77 0.352
100
HRW001 Hair Whorl 35 0.352
101
BRC012 Brucellosis 66 0.352
102
PRP027 Peripheral Vascular Disease 71 0.352
103
c ACT073 Acute Leukemia 59 0.352
104
PNC001 Pancytopenia 52 0.352
105
LVR012 Liver Cirrhosis 62 0.352
106
NNT012 Neonatal Jaundice 53 0.352
107
P ECL001 Eclampsia 52 0.352
108
ALC006 Alcoholic Hepatitis 61 0.352
109
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.352
110
c LKM063 Leukemia, Chronic Myeloid 71 0.321
111
P FML018 Familial Mediterranean Fever 73 0.321
112
c CNT035 Central Nervous System Disease 53 0.321
113
BRS051 Breast Disease 58 0.321
114
P NRV007 Nervous System Disease 66 0.321
115
P LYM118 Lymphoma 69 0.287
116
ACQ007 Acquired Immunodeficiency Syndrome 58 0.287
117
MYC087 Mycoplasma Pneumoniae Pneumonia 52 0.287
118
GNG013 Gingivitis 59 0.287
119
TRN015 Transient Cerebral Ischemia 62 0.287
120
P BNG032 Benign Mesothelioma 53 0.287
121
PLR007 Pleural Empyema 51 0.287
122
CRH001 Crohn's Disease 80 0.287
123
P RBL001 Rubella 58 0.287
124
c BCT013 Bacterial Pneumonia 47 0.287
125
c ALT008 Alternating Hemiplegia of Childhood 1 39 0.249
126
HLX001 Helix Syndrome 47 0.249
127
DFC004 Deficiency Anemia 74 0.249
128
TYP007 Typhoid Fever 63 0.249
129
P GRV001 Graves' Disease 54 0.249
130
CHR063 Chronic Mucocutaneous Candidiasis 68 0.249
131
RYN005 Raynaud Phenomenon 45 0.249
132
P PLV020 Pelvic Organ Prolapse 58 0.203
133
c TYP009 Type 2 Diabetes Mellitus 92 0.203
134
BCT022 Bacterial Infectious Disease 56 0.203
135
P KLZ004 Kala-Azar 1 41 0.203
136
ISC004 Ischemia 61 0.203
137
P PLY011 Polycystic Ovary Syndrome 57 0.203
138
P THY032 Thyroiditis 56 0.203
139
VSC003 Visceral Leishmaniasis 54 0.203
140
LSH001 Leishmaniasis 63 0.203
141
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.144
142
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.144
143
TKY002 Takayasu Arteritis 61 0.144
144
MJD001 Majeed Syndrome 39 0.144
145
MYL009 Myelodysplastic Syndrome 67 0.144
146
P GRF003 Graft-Versus-Host Disease 71 0.144
148
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.144
149
ALC007 Alcohol Dependence 65 0.144
150
P APL001 Aplastic Anemia 73 0.144
151
SCK003 Sickle Cell Anemia 74 0.144
152
MVL001 Mevalonic Aciduria 65 0.144
153
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 0.144
154
ATM095 Autoimmune Disease 61 0.144
155
c SPN291 Spinocerebellar Ataxia 7 50 0.144
156
P MTR004 Maturity-Onset Diabetes of the Young 66 0.144
157
MCK007 Muckle-Wells Syndrome 64 0.144
158
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.144
159
P INF032 Infertility 60 0.144
160
ORC001 Orchitis 44 0.144
161
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.144
162
46X002 46 Xx Gonadal Dysgenesis 38 0.144
163
P MLN007 Male Infertility 56 0.144
164
NNT024 Neonatal Stroke 31 0.144
165
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 53 0.144
166
HYP266 Hypoxia 56 0.144
167
CRV002 Cervix Uteri Carcinoma in Situ 48 0.144
168
P DCR003 Dacryoadenitis 44 0.144
169
WLL006 Wells Syndrome 49 0.144
170
CRV045 Cervical Intraepithelial Neoplasia 38 0.144
171
ALL014 Allergic Encephalomyelitis 34 0.144
172
ANC002 Anca-Associated Vasculitis 44 0.144
173
P DBT009 Diabetes Mellitus 67 0.144
174
c CHR417 Chronic Graft Versus Host Disease 55 0.144
175
NDL013 Nodular Regenerative Hyperplasia 46 0.144
176
c ACT135 Acute Graft Versus Host Disease 51 0.144
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