Search results for dvl3

129 hits were found for dvl3

# Family MCID Name MIFTS Score
1
c RBN020 Robinow Syndrome, Autosomal Dominant 3 35 35.369
2
P RBN002 Robinow Syndrome 56 34.408
3
c ATS082 Autosomal Dominant Robinow Syndrome 46 31.325
4
c RBN018 Robinow Syndrome, Autosomal Dominant 1 51 21.184
5
c RBN022 Robinow Syndrome, Autosomal Recessive 1 57 21.184
6
P HPT023 Hepatocellular Carcinoma 95 16.283
7
NRL016 Neural Tube Defects 80 14.092
8
c RBN017 Robinow Syndrome, Autosomal Dominant 2 45 13.841
9
DBL002 Double Outlet Right Ventricle 56 8.221
10
INT395 Intracranial Meningioma 47 8.123
11
P STR020 Strabismus 56 8.083
12
c BRC052 Brachydactyly, Type B2 40 7.822
13
c BRC051 Brachydactyly, Type B1 50 7.822
14
P EXD001 Exudative Vitreoretinopathy 56 7.822
15
P BRS047 Breast Cancer 97 1.932
16
P PRS040 Prostate Cancer 95 1.845
17
P CLR023 Colorectal Cancer 100 1.680
18
MNT002 Mental Depression 56 1.643
19
SQM006 Squamous Cell Carcinoma 59 1.352
20
CRV035 Cervical Cancer 72 1.292
21
c PCH010 Pachyonychia Congenita 3 43 1.201
22
P ADN016 Adenocarcinoma 63 1.175
23
MSM003 Mesomelia 17 1.175
24
P BLD134 Bladder Cancer 79 1.148
25
SPP011 Suppression of Tumorigenicity 12 61 1.148
26
P GLM040 Glioma Susceptibility 1 70 1.148
27
MLG169 Malignant Astrocytoma 57 1.148
28
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 59 1.132
29
c CLR087 Colorectal Cancer 12 34 1.132
30
GST103 Gastric Cancer, Hereditary Diffuse 68 1.132
31
SML009 Small Intestine Adenocarcinoma 57 1.132
32
P MJR001 Major Depressive Disorder 68 1.086
33
GLB002 Glioblastoma 67 1.086
34
DPR016 Depression 64 1.086
35
P MCR010 Microcephaly 59 1.050
36
c MCR322 Microcephaly 18, Primary, Autosomal Dominant 34 0.962
37
MCR257 Microcephaly, Amish Type 35 0.962
38
c PRM212 Primary Microcephaly 40 0.962
39
P PNC035 Pancreatic Cancer 87 0.904
40
P NRB001 Neuroblastoma 66 0.900
41
TRT001 Teratocarcinoma 41 0.723
42
P OVR042 Ovarian Cancer 88 0.683
43
BRS099 Breast Ductal Carcinoma 61 0.654
44
LNG039 Lung Squamous Cell Carcinoma 57 0.654
45
LNG012 Lung Occult Squamous Cell Carcinoma 20 0.654
46
LNG007 Lung Mixed Small Cell and Squamous Cell Carcinoma 20 0.654
47
P LNG032 Lung Cancer 98 0.533
48
c HPT016 Hepatitis B 62 0.337
49
BRN034 Brain Meningioma 33 0.301
50
P FML011 Familial Adenomatous Polyposis 70 0.301
51
P LKM062 Leukemia, Acute Lymphoblastic 69 0.301
52
MNN043 Meningioma, Familial 79 0.301
53
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.301
54
P VNT002 Ventricular Septal Defect 58 0.301
55
P LKM002 Leukemia 65 0.301
56
RTN020 Retinal Vascular Disease 45 0.301
57
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.301
58
SCR001 Secretory Meningioma 40 0.301
59
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.301
60
P THR014 Thrombocytopenia 66 0.301
61
P MYS005 Myositis 55 0.261
62
INC002 Inclusion Body Myositis 56 0.261
63
CLF027 Cleft Palate, Isolated 64 0.261
64
P GST044 Gastritis 55 0.261
65
MCH006 Mechanical Strabismus 40 0.261
66
P SCL018 Scoliosis 57 0.213
67
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.213
68
MYL009 Myelodysplastic Syndrome 67 0.213
69
P LYM118 Lymphoma 66 0.213
70
P INF037 Inflammatory Bowel Disease 53 0.213
71
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.213
72
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.213
73
P OST002 Osteoporosis 76 0.213
74
OST159 Osteogenic Sarcoma 66 0.213
75
c LKM061 Leukemia, Acute Myeloid 83 0.213
76
c RBN023 Robinow Syndrome, Autosomal Recessive 2 26 0.213
77
P BRC006 Brachydactyly 52 0.213
78
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.213
79
P GST053 Gastric Cancer 82 0.213
80
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.213
81
NRD079 Neurodevelopmental Disorder with Structural Brain Anomalies and Dysmorphic Facies 21 0.213
82
FTL006 Fetal Alcohol Spectrum Disorder 43 0.213
83
ANN002 Anencephaly 57 0.213
84
c NLD006 Nail Disorder, Nonsyndromic Congenital, 9 36 0.213
85
CHL065 Cholangiocarcinoma 57 0.213
86
ESP021 Esophageal Cancer 84 0.213
87
INT079 Intrahepatic Cholangiocarcinoma 51 0.213
88
CLF001 Cleft Lip 54 0.213
89
CRN088 Craniorachischisis 35 0.213
91
PNS014 Penis Agenesis 38 0.213
92
CLF004 Cleft Lip/palate 56 0.213
93
P SCL048 Sclerosteosis 58 0.151
94
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.151
95
ORL015 Oral Squamous Cell Carcinoma 43 0.151
96
VLC001 Velocardiofacial Syndrome 57 0.151
97
c MCR241 Microphthalmia, Syndromic 3 56 0.151
98
LYM133 Lymphoma, Hodgkin, Classic 69 0.151
99
SRC027 Sarcoma, Synovial 58 0.151
100
P ASP001 Asperger Syndrome 48 0.151
101
c 46X055 46,xy Sex Reversal 3 40 0.151
102
c DPH024 Diaphragmatic Hernia, Congenital 63 0.151
103
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.151
104
P GRF003 Graft-Versus-Host Disease 71 0.151
105
P LKM071 Leukemia, Chronic Lymphocytic 74 0.151
106
HYP748 Hypertelorism 46 0.151
107
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.151
108
c LNG109 Lung Cancer Susceptibility 1 26 0.151
109
c RTN041 Retinitis Pigmentosa 11 43 0.151
110
FRY006 Fryns Microphthalmia Syndrome 52 0.151
111
P LNG064 Lung Cancer Susceptibility 3 69 0.151
112
DFF005 Diffuse Large B-Cell Lymphoma 55 0.151
113
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.151
114
OST015 Osteochondrodysplasia 60 0.151
115
SKN022 Skin Squamous Cell Carcinoma 53 0.151
116
P DSR090 Disorder of Sexual Development 45 0.151
117
HRT011 Heart Septal Defect 49 0.151
118
SPN035 Spindle Cell Sarcoma 51 0.151
119
MCR013 Microphthalmia 59 0.151
120
SRC014 Sarcoma 64 0.151
121
PRT037 Pertussis 49 0.151
122
P BCL017 B-Cell Lymphoma 57 0.151
123
c SPR009 Sporadic Breast Cancer 42 0.151
124
HYP082 Hypopharynx Cancer 47 0.151
125
OST012 Osteoarthritis 77 0.151
126
SX2004 Sox2 Disorder 13 0.151
127
P SYN140 Syndrome with 46,xy Disorder of Sex Development 23 0.151
128
CLP005 Ciliopathy 40 0.151
129
DWR001 Dwarfism 44 0.151
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