Search results for wnt7a

208 hits were found for wnt7a

# Family MCID Name MIFTS Score
1
ULN017 Ulna and Fibula, Absence of, with Severe Limb Deficiency 35 35.589
2
FBL008 Fibular Aplasia or Hypoplasia, Femoral Bowing and Poly-, Syn-, and Oligodactyly 43 33.460
3
END057 Endometrial Cancer 71 17.140
4
P CLR023 Colorectal Cancer 100 16.870
5
P GST053 Gastric Cancer 82 16.472
6
P HPT023 Hepatocellular Carcinoma 95 15.996
7
P PHC014 Phocomelia 23 14.604
8
CLB002 Clubfoot 51 11.924
9
P FRG001 Fragile X Syndrome 70 11.462
10
c EXD008 Exudative Vitreoretinopathy 1 71 10.582
11
NRR002 Norrie Disease 60 8.513
12
P EXD001 Exudative Vitreoretinopathy 55 8.513
13
AML065 Amelia 29 8.488
14
TTH002 Tooth Agenesis 61 8.399
15
SNT006 Santos Syndrome 16 8.319
16
P MYR002 Mayer-Rokitansky-Kuster-Hauser Syndrome 60 7.872
17
P PRS049 Persistent Mullerian Duct Syndrome 52 7.721
18
FCL009 Focal Dermal Hypoplasia 64 7.620
19
MLL011 Mullerian Aplasia and Hyperandrogenism 45 7.483
20
DPN005 Du Pan Syndrome 47 7.483
21
TBH001 Tibia, Hypoplasia or Aplasia of, with Polydactyly 46 7.483
22
P LNG032 Lung Cancer 98 2.501
23
P OVR042 Ovarian Cancer 88 2.442
24
c SML038 Small Cell Cancer of the Lung 69 2.131
25
SQM006 Squamous Cell Carcinoma 59 1.925
26
P BRS047 Breast Cancer 97 1.845
27
BLD170 Bladder Exstrophy and Epispadias Complex 42 1.772
28
BLD129 Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex 41 1.772
29
CLB026 Colobomatous Microphthalmia 46 1.634
30
ORL015 Oral Squamous Cell Carcinoma 43 1.595
31
P ADN016 Adenocarcinoma 63 1.581
32
P LKM062 Leukemia, Acute Lymphoblastic 69 1.552
33
CLR109 Colorectal Adenocarcinoma 50 1.537
34
ADN018 Adenoma 58 1.537
35
P BLD134 Bladder Cancer 79 1.474
36
P MSC005 Muscular Dystrophy 66 1.457
37
P BNG032 Benign Mesothelioma 53 1.422
38
MSC157 Muscular Dystrophy, Duchenne Type 79 1.422
39
P END044 Endometriosis 62 1.403
40
P MSC003 Muscular Atrophy 52 1.342
41
ATS010 Autosomal Recessive Disease 42 1.271
42
ANX010 Anxiety 70 1.215
43
ESP021 Esophageal Cancer 84 1.182
44
CLR108 Colorectal Adenoma 63 1.137
45
OST012 Osteoarthritis 77 1.137
46
c CLR085 Colorectal Cancer 1 42 1.118
47
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.118
48
TNG009 Tongue Squamous Cell Carcinoma 43 1.076
49
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 1.076
50
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 1.076
51
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.054
52
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.054
53
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.054
54
P EST001 Estrogen-Receptor Positive Breast Cancer 49 1.054
55
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.054
56
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.054
57
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.054
58
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.054
59
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.054
60
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.054
61
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.054
62
HYP066 Hyperglycemia 60 1.054
63
MLG079 Malignant Pleural Mesothelioma 42 1.054
65
P VTR007 Vitreoretinopathy 45 1.030
66
HYP043 Hyperandrogenism 47 1.005
67
CRV035 Cervical Cancer 72 0.978
68
ADR040 Adrenal Gland Pheochromocytoma 45 0.978
69
P PHC003 Pheochromocytoma 70 0.978
70
P PNC035 Pancreatic Cancer 86 0.970
71
c TYP009 Type 2 Diabetes Mellitus 92 0.949
72
LMY014 Leiomyoma, Uterine 55 0.949
73
CLB019 Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly 43 0.949
74
LMY002 Leiomyoma 51 0.949
75
P MCR010 Microcephaly 59 0.949
76
SYN005 Synostosis 43 0.949
77
GLM045 Glioma 62 0.949
78
GLL048 Glial Tumor 52 0.949
79
TRD003 Taurodontism 30 0.916
80
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.916
81
P PLY011 Polycystic Ovary Syndrome 57 0.916
82
P PLY006 Polydactyly 58 0.916
83
P SCH015 Schizophrenia 74 0.880
84
PRG014 Progesterone Resistance 42 0.880
85
P CRN024 Corneal Disease 43 0.880
86
ANV001 Anovulation 46 0.880
87
STR067 Stroke, Ischemic 79 0.880
88
HMR015 Humeroradial Synostosis 36 0.836
89
P BRC006 Brachydactyly 52 0.836
90
P PLY014 Polycystic Kidney Disease 71 0.779
91
FBL010 Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome 24 0.779
92
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.779
93
P KDN018 Kidney Disease 72 0.779
94
P PRS040 Prostate Cancer 95 0.712
95
c CLR087 Colorectal Cancer 12 34 0.523
96
GST103 Gastric Cancer, Hereditary Diffuse 68 0.523
97
SML009 Small Intestine Adenocarcinoma 57 0.523
98
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 0.523
99
MYL005 Myelofibrosis 70 0.517
100
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.435
101
P LTR001 Lateral Sclerosis 58 0.435
102
END062 Endometrial Hyperplasia 48 0.413
103
P LNG064 Lung Cancer Susceptibility 3 70 0.364
104
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.337
105
CLF027 Cleft Palate, Isolated 64 0.308
106
PRT251 Proteinuria, Chronic Benign 58 0.275
107
c HYP836 Hypercholesterolemia, Familial, 1 73 0.275
108
P PLM036 Pulmonary Fibrosis 65 0.275
109
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.238
110
TBL029 Tubulin, Beta 28 0.238
111
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.238
112
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.238
113
c SPL067 Split-Hand/foot Malformation 1 46 0.238
114
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.238
115
RNL077 Renal Fibrosis 46 0.238
116
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.238
117
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.238
118
END007 Endosalpingiosis 37 0.238
119
CLN015 Colon Adenocarcinoma 64 0.238
120
PSD009 Pseudohermaphroditism 47 0.238
121
P NSP012 Nasopharyngeal Carcinoma 60 0.238
122
LMB050 Limbal Stem Cell Deficiency 50 0.238
123
P ALP008 Alopecia 53 0.238
124
P AVS003 Avascular Necrosis 41 0.238
125
ISL121 Isolated Split Hand-Split Foot Malformation 42 0.238
126
P JBR020 Joubert Syndrome 1 74 0.195
127
MSC007 Muscle Hypertrophy 64 0.195
128
P ANR048 Aniridia 1 66 0.195
129
P FML011 Familial Adenomatous Polyposis 71 0.195
130
NLP001 Nail-Patella Syndrome 63 0.195
131
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.195
132
KRT008 Keratopathy 46 0.195
133
PNC129 Pancreatic Adenocarcinoma 65 0.195
134
LNG039 Lung Squamous Cell Carcinoma 57 0.195
135
OVR094 Ovarian Epithelial Cancer 39 0.195
136
BRN071 Brain Injury 50 0.195
137
LNG099 Lung Disease 62 0.195
138
P SCK005 Sickle Cell Disease 56 0.195
139
HMM005 Hemimelia 33 0.195
140
CLP005 Ciliopathy 41 0.195
141
P ALP061 Alopecia, Androgenetic, 1 49 0.138
142
P SRC025 Sarcoidosis 1 70 0.138
143
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.138
144
AGN016 Aging 54 0.138
145
P AST005 Asthma 76 0.138
146
INS024 Insulin-Like Growth Factor I 77 0.138
147
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.138
148
GNT031 Genitopatellar Syndrome 42 0.138
149
HYP020 Hyperprolactinemia 63 0.138
150
P INF037 Inflammatory Bowel Disease 53 0.138
151
P END046 Endometritis 46 0.138
152
MCR013 Microphthalmia 60 0.138
153
CRB004 Cerebral Artery Occlusion 46 0.138
154
TNG007 Tongue Carcinoma 55 0.138
155
BLD130 Bladder Exstrophy 44 0.138
156
c CHR711 Chronic Asthma 41 0.138
157
P SPL061 Split Hand-Foot Malformation 42 0.138
158
P PLY147 Polydactyly, Postaxial, Type A1 50 0.138
159
PLY150 Polykaryocytosis Inducer 29 0.138
160
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.138
161
AND014 Androgenic Alopecia 46 0.138
162
c ORF048 Orofacial Cleft 1 30 0.138
163
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.138
164
c SCL052 Scleroderma, Familial Progressive 60 0.138
165
NRL016 Neural Tube Defects 81 0.138
166
c MJR024 Major Affective Disorder 9 40 0.138
167
c MYS019 Miyoshi Muscular Dystrophy 2 19 0.138
168
c MJR022 Major Affective Disorder 8 37 0.138
169
P ATS364 Autism 72 0.138
170
P BND020 Bone Disease 60 0.138
171
ISC004 Ischemia 61 0.138
172
END041 Endometrial Adenocarcinoma 63 0.138
173
P ACN011 Acne 55 0.138
174
URT010 Ureteral Obstruction 45 0.138
175
P INF032 Infertility 60 0.138
176
P HYP040 Hypospadias 51 0.138
177
AMN001 Amenorrhea 53 0.138
178
AZS001 Azoospermia 45 0.138
179
P GND004 Gonadal Dysgenesis 46 0.138
180
P MLN007 Male Infertility 56 0.138
181
INT066 Interstitial Lung Disease 60 0.138
182
PLS011 Plasmacytoma 56 0.138
183
HRM002 Hermaphroditism 35 0.138
184
P BPL003 Bipolar Disorder 56 0.138
185
P ART021 Arteriosclerosis 53 0.138
186
OST159 Osteogenic Sarcoma 66 0.138
187
RDL037 Radial Ray Deficiency, X-Linked 16 0.138
188
TCK004 Tick Infestation 29 0.138
189
P NRB001 Neuroblastoma 66 0.138
190
c CHR684 Chronic Kidney Disease 74 0.138
191
CRB209 Cerebellar Malformation 22 0.138
192
PTT037 Pituitary Tumors 44 0.138
193
HYP266 Hypoxia 56 0.138
194
c 46X011 46, Xy Disorders of Sexual Development 20 0.138
195
CLF001 Cleft Lip 54 0.138
196
P MYP004 Myopathy 67 0.138
197
P HLP001 Holoprosencephaly 69 0.138
198
TRM010 Traumatic Brain Injury 50 0.138
199
P BCL017 B-Cell Lymphoma 57 0.138
201
P ALP009 Alopecia Areata 59 0.138
202
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.138
203
DFF035 Diffuse Cutaneous Systemic Sclerosis 45 0.138
204
SPT023 Septate Uterus 30 0.138
205
CLF056 Cleft Lip with or Without Cleft Palate 43 0.138
206
UTR054 Uterine Hypoplasia 21 0.138
207
CNG587 Congenital Limb Malformation 12 0.138
208
THY029 Thyroid Carcinoma 54 0.138
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