Search results for rpa1

117 hits were found for rpa1

# Family MCID Name MIFTS Score
1
P ATX030 Ataxia-Telangiectasia 80 16.647
2
XRD010 Xeroderma Pigmentosum, Variant Type 72 13.639
3
WRN001 Werner Syndrome 69 13.332
4
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 11.192
5
P NJM001 Nijmegen Breakage Syndrome 75 11.039
6
P CCK001 Cockayne Syndrome 67 11.039
7
BLM001 Bloom Syndrome 65 10.885
8
c FNC027 Fanconi Anemia, Complementation Group a 80 8.103
9
c ALP101 Alpha-Thalassemia 62 7.697
10
c CCK008 Cockayne Syndrome a 59 7.697
11
c ALZ059 Alzheimer Disease 13 26 7.697
12
ALP100 Alpha-Thalassemia/mental Retardation Syndrome, X-Linked 62 7.697
13
c MYS055 Myasthenic Syndrome, Congenital, 6, Presynaptic 49 7.697
14
c HYP525 Hypotrichosis 2 40 7.697
15
P CNG001 Congenital Myasthenic Syndrome 68 7.697
16
HVR001 Haverhill Fever 32 7.697
17
ESP021 Esophageal Cancer 84 2.066
18
HLX001 Helix Syndrome 47 1.765
19
P NSP012 Nasopharyngeal Carcinoma 60 1.539
20
P HPT023 Hepatocellular Carcinoma 95 1.350
21
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.304
22
TLN003 Telangiectasis 51 1.253
23
P CLR023 Colorectal Cancer 100 1.225
24
c ATS007 Autism Spectrum Disorder 71 1.162
25
c SML038 Small Cell Cancer of the Lung 68 1.162
26
P FBR017 Fibrosarcoma 55 1.162
27
P LNG032 Lung Cancer 98 1.125
28
P GST053 Gastric Cancer 82 1.084
29
P PNC035 Pancreatic Cancer 87 0.933
30
P BRS047 Breast Cancer 97 0.894
31
THY124 Thyroid Gland Papillary Carcinoma 38 0.866
32
P ATS364 Autism 72 0.551
33
SZR001 Sezary's Disease 60 0.551
34
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.434
35
BLD131 Bladder Urothelial Carcinoma 59 0.406
36
DFC004 Deficiency Anemia 74 0.307
37
CHG001 Chagas Disease 65 0.307
38
P ALZ034 Alzheimer Disease 87 0.266
39
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.266
40
KPS004 Kaposi Sarcoma 76 0.266
41
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.266
42
P TMR010 Tumor Predisposition Syndrome 69 0.266
43
P LKM071 Leukemia, Chronic Lymphocytic 74 0.266
44
c SPN294 Spinocerebellar Ataxia 1 53 0.266
45
MLD018 Mild Cognitive Impairment 48 0.266
46
P MLT074 Multiple Endocrine Neoplasia 58 0.266
47
SPN035 Spindle Cell Sarcoma 51 0.266
48
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.266
49
SRC014 Sarcoma 64 0.266
50
P BCL017 B-Cell Lymphoma 57 0.266
51
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 0.266
52
INH023 Inherited Cancer-Predisposing Syndrome 53 0.266
53
c SYS001 Systemic Lupus Erythematosus 85 0.217
54
P SCK004 Seckel Syndrome 58 0.217
55
c THY107 Thymoma, Familial 42 0.217
56
P HNT016 Huntington Disease 73 0.217
57
NND010 Nondisjunction 34 0.217
58
DFF005 Diffuse Large B-Cell Lymphoma 55 0.217
59
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.217
60
P FLL037 Follicular Lymphoma 66 0.217
61
P LKM002 Leukemia 65 0.217
62
P THY023 Thymoma 64 0.217
63
FDL002 Food Allergy 47 0.217
64
GLB002 Glioblastoma 67 0.217
65
SQM006 Squamous Cell Carcinoma 59 0.217
66
P BNC003 Bone Cancer 58 0.217
67
P LYN001 Lynch Syndrome 76 0.217
68
HYP082 Hypopharynx Cancer 47 0.217
69
P LPS004 Lupus Erythematosus 61 0.217
70
HYP266 Hypoxia 56 0.217
71
THY029 Thyroid Carcinoma 55 0.217
72
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.154
73
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.154
74
P CTN015 Cutaneous T Cell Lymphoma 48 0.154
75
P PTS002 Ptosis 52 0.154
76
WLL001 Williams-Beuren Syndrome 60 0.154
77
P OVR042 Ovarian Cancer 88 0.154
78
c MCR247 Microcephaly 1, Primary, Autosomal Recessive 42 0.154
79
OST159 Osteogenic Sarcoma 66 0.154
80
AGN016 Aging 53 0.154
81
c HPT073 Hepatitis C Virus 70 0.154
82
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.154
83
P LSS002 Lissencephaly 52 0.154
84
c FNC032 Fanconi Anemia, Complementation Group B 48 0.154
85
c TYP008 Type 1 Diabetes Mellitus 77 0.154
86
P MYS003 Myasthenia Gravis 67 0.154
87
MLL018 Miller-Dieker Lissencephaly Syndrome 53 0.154
88
c FNC028 Fanconi Anemia, Complementation Group L 46 0.154
89
c LKM063 Leukemia, Chronic Myeloid 70 0.154
90
SMT018 Smith-Mccort Dysplasia 2 34 0.154
91
ATM095 Autoimmune Disease 61 0.154
92
EPC005 Epicanthus 35 0.154
93
c CCK007 Cockayne Syndrome B 56 0.154
94
P FNC044 Fanconi Anemia, Complementation Group C 56 0.154
95
P LNG064 Lung Cancer Susceptibility 3 69 0.154
96
c PRM212 Primary Microcephaly 40 0.154
97
BLP004 Blepharophimosis 36 0.154
98
PPL002 Papillary Carcinoma 46 0.154
99
P BNG032 Benign Mesothelioma 53 0.154
100
P MLN007 Male Infertility 56 0.154
101
c HPT001 Hepatitis C 61 0.154
102
P ADN016 Adenocarcinoma 63 0.154
103
P SKN015 Skin Carcinoma 71 0.154
104
P MCR010 Microcephaly 59 0.154
105
P NTR004 Neutropenia 62 0.154
106
P THR014 Thrombocytopenia 66 0.154
107
BRN028 Brain Cancer 73 0.154
108
P INF032 Infertility 60 0.154
109
P MYL006 Myeloid Leukemia 60 0.154
110
P MYT002 Myotonic Dystrophy 51 0.154
111
P NRC002 Narcolepsy 55 0.154
112
DRM011 Dermatophytosis 52 0.154
113
GLM045 Glioma 62 0.154
114
DFF036 Differentiated Thyroid Carcinoma 51 0.154
115
HYP056 Hypoglycemia 65 0.154
116
GLL048 Glial Tumor 51 0.154
117
PRM329 Premature Aging 36 0.154
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