Search results for wnt10a

164 hits were found for wnt10a

# Family MCID Name MIFTS Score
1
ODN009 Odontoonychodermal Dysplasia 35 89.363
2
TTH002 Tooth Agenesis 61 54.107
3
c TTH013 Tooth Agenesis, Selective, 4 27 53.648
4
SCH038 Schopf-Schulz-Passarge Syndrome 51 52.868
5
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 68 20.631
6
P CLR023 Colorectal Cancer 100 20.158
7
P ECT006 Ectodermal Dysplasia 62 19.610
8
ECT070 Ectodermal Dysplasia 1, Hypohidrotic, X-Linked 61 19.050
9
P HYP087 Hypotrichosis 41 12.583
10
c EXD008 Exudative Vitreoretinopathy 1 71 10.724
11
HYP206 Hypohidrotic Ectodermal Dysplasia Autosomal Recessive 35 9.744
12
TRD003 Taurodontism 30 9.648
13
AND001 Anodontia 42 8.714
14
AND014 Androgenic Alopecia 46 8.020
15
FBL008 Fibular Aplasia or Hypoplasia, Femoral Bowing and Poly-, Syn-, and Oligodactyly 43 7.729
16
NRR002 Norrie Disease 60 7.583
17
FCL009 Focal Dermal Hypoplasia 64 7.583
18
P EXD001 Exudative Vitreoretinopathy 55 7.583
19
P ORF002 Orofacial Cleft 42 7.583
20
PLM029 Palmoplantar Keratosis 48 3.072
21
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.946
22
HRW001 Hair Whorl 35 1.919
23
KRT009 Keratosis 52 1.800
24
P OVR042 Ovarian Cancer 88 1.705
25
CLF027 Cleft Palate, Isolated 64 1.704
26
ECT061 Ectodermal Dysplasia 10a, Hypohidrotic/hair/nail Type, Autosomal Dominant 48 1.704
27
BLD170 Bladder Exstrophy and Epispadias Complex 42 1.659
28
BLD129 Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex 41 1.659
29
c ATS013 Autosomal Recessive Congenital Ichthyosis 65 1.605
30
P ALP008 Alopecia 53 1.599
31
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.551
32
P RCT021 Rectum Cancer 54 1.551
33
P PLM036 Pulmonary Fibrosis 65 1.551
34
STF002 Stiff Skin Syndrome 53 1.513
35
ATS010 Autosomal Recessive Disease 42 1.376
36
ANH002 Anhidrosis 45 1.376
37
CLF001 Cleft Lip 54 1.353
38
END057 Endometrial Cancer 71 1.346
39
CLF004 Cleft Lip/palate 57 1.273
40
P OVR082 Overgrowth Syndrome 42 1.248
41
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.173
42
ESP021 Esophageal Cancer 84 1.131
43
TRT001 Teratocarcinoma 41 1.131
44
INT067 Interstitial Nephritis 47 1.108
45
P TTH010 Tooth Agenesis, Selective, 1 30 1.085
46
BRK010 Burkitt Lymphoma 66 1.085
47
MCN001 Mucinous Adenocarcinoma 49 1.085
48
SQM006 Squamous Cell Carcinoma 59 1.085
49
APP009 Appendix Adenocarcinoma 47 1.085
50
OLG005 Oligodontia-Colorectal Cancer Syndrome 29 1.060
51
c TTH025 Tooth Agenesis, Selective, 9 18 1.033
52
c BRN108 Branchiootic Syndrome 1 63 1.004
53
LVR012 Liver Cirrhosis 62 1.004
54
CLF056 Cleft Lip with or Without Cleft Palate 43 1.004
55
BNR002 Bone Resorption Disease 47 0.973
56
P FML011 Familial Adenomatous Polyposis 71 0.973
57
AND017 Anodontia of Permanent Dentition 25 0.973
58
RGN005 Regional Odontodysplasia 26 0.973
59
P PRS040 Prostate Cancer 95 0.940
60
P LNG032 Lung Cancer 98 0.940
61
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.939
62
ECT094 Ectodermal Dysplasia 12, Hypohidrotic/hair/tooth/nail Type 19 0.939
63
c ECT072 Ectodermal Dysplasia 11a, Hypohidrotic/hair/tooth Type, Autosomal Dominant 35 0.939
64
P KRT007 Keratoconus 50 0.939
65
c ECT058 Ectodermal Dysplasia 11b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 40 0.939
66
P EPD016 Epidermolysis Bullosa 53 0.939
67
CHL078 Childhood-Onset Schizophrenia 29 0.939
68
ERY069 Erythrokeratoderma ''en Cocardes'' 26 0.939
69
RRG043 Rare Genetic Skin Disease 17 0.939
70
THY029 Thyroid Carcinoma 54 0.939
71
c MCR261 Microphthalmia, Syndromic 2 50 0.900
72
MCR013 Microphthalmia 60 0.900
73
P SYN165 Syndromic Microphthalmia 34 0.900
74
c AML047 Amelogenesis Imperfecta, Type Ia 33 0.900
75
c DFN269 Deafness, Autosomal Recessive 98 36 0.900
76
GLB002 Glioblastoma 67 0.900
77
P GND004 Gonadal Dysgenesis 46 0.900
78
P TRN020 Turner Syndrome 67 0.900
79
P AML002 Amelogenesis Imperfecta 56 0.900
80
P JNC001 Junctional Epidermolysis Bullosa 53 0.900
81
c DFN280 Deafness, Autosomal Recessive 35 0.900
82
HDR007 Hidrotic Ectodermal Dysplasia 2 21 0.900
83
47X002 47,xyy 48 0.900
84
c NLD006 Nail Disorder, Nonsyndromic Congenital, 9 35 0.854
85
CLR108 Colorectal Adenoma 63 0.854
86
ADN018 Adenoma 58 0.854
87
P LMY004 Leiomyosarcoma 62 0.793
88
P BRS047 Breast Cancer 97 0.753
89
P PNC035 Pancreatic Cancer 86 0.753
90
P GST053 Gastric Cancer 82 0.733
91
P SCL018 Scoliosis 57 0.648
92
P LNG064 Lung Cancer Susceptibility 3 70 0.613
93
P ALP061 Alopecia, Androgenetic, 1 49 0.437
94
OST012 Osteoarthritis 77 0.412
95
KLD004 Keloid Disorder 39 0.412
96
P TMR010 Tumor Predisposition Syndrome 69 0.407
97
ADN011 Adenoid Cystic Carcinoma 68 0.407
98
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.407
99
BLD173 Bladder Small Cell Carcinoma 44 0.407
100
ADN089 Adenosquamous Lung Carcinoma 49 0.407
101
LNG019 Lung Combined Type Small Cell Carcinoma 32 0.407
102
LNG039 Lung Squamous Cell Carcinoma 57 0.407
103
GST040 Gastric Adenocarcinoma 66 0.407
104
P LNG021 Lung Occult Small Cell Carcinoma 20 0.407
105
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.407
106
LNG099 Lung Disease 62 0.385
107
HLC007 Helicobacter Pylori Infection 67 0.326
108
WTK002 Witkop Syndrome 43 0.326
109
RNL077 Renal Fibrosis 46 0.252
110
CHL065 Cholangiocarcinoma 58 0.252
111
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.252
112
INT079 Intrahepatic Cholangiocarcinoma 51 0.252
113
DNT012 Dental Caries 53 0.252
114
HYP080 Hypogonadism 49 0.252
115
DRM006 Dermatitis 62 0.252
116
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.206
117
P OST002 Osteoporosis 77 0.206
118
c TRC092 Trichorhinophalangeal Syndrome, Type I 54 0.206
119
ORL015 Oral Squamous Cell Carcinoma 43 0.206
120
ADR040 Adrenal Gland Pheochromocytoma 45 0.206
121
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.206
122
P PHC003 Pheochromocytoma 70 0.206
123
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.206
124
P LKM071 Leukemia, Chronic Lymphocytic 74 0.206
125
CHL068 Cholestasis 61 0.206
126
P INT143 Interstitial Cystitis 59 0.206
127
P CYS018 Cystitis 59 0.206
128
LYM133 Lymphoma, Hodgkin, Classic 74 0.146
129
c ALB021 Albinism, Oculocutaneous, Type Ii 58 0.146
130
CRV035 Cervical Cancer 72 0.146
131
LYM143 Lymphoma, Non-Hodgkin, Familial 79 0.146
132
c TTH026 Tooth Agenesis, Selective, 7 17 0.146
133
ECT095 Ectodermal Dysplasia 13, Hair/tooth Type 18 0.146
134
PRT251 Proteinuria, Chronic Benign 58 0.146
135
c PRC016 Pre-Eclampsia 64 0.146
136
BLD130 Bladder Exstrophy 44 0.146
137
ASP027 Asparagus, Specific Smell Hypersensitivity 7 0.146
138
c DNT051 Dentin Dysplasia, Type I 33 0.146
139
c ATS007 Autism Spectrum Disorder 72 0.146
140
P LYM118 Lymphoma 69 0.146
141
CLR109 Colorectal Adenocarcinoma 50 0.146
142
c OVR114 Ovarian Cancer 1 60 0.146
143
BRT054 Brittle Bone Disorder 74 0.146
144
c BRS110 Breast-Ovarian Cancer, Familial 1 58 0.146
145
c HPT073 Hepatitis C Virus 71 0.146
146
c SCL052 Scleroderma, Familial Progressive 60 0.146
147
P ATS364 Autism 72 0.146
148
P BND020 Bone Disease 60 0.146
149
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 0.146
150
P ACN011 Acne 55 0.146
151
c HPT001 Hepatitis C 61 0.146
152
RTR008 Root Resorption 44 0.146
153
TXC005 Toxic Shock Syndrome 62 0.146
154
SKN016 Skin Disease 62 0.146
155
INT066 Interstitial Lung Disease 60 0.146
156
P OLG002 Oligodendroglioma 66 0.146
157
EMB004 Embryonal Carcinoma 55 0.146
158
P DNT011 Dentinogenesis Imperfecta 52 0.146
159
P DNT009 Dentin Dysplasia 40 0.146
160
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 68 0.146
161
P MYP004 Myopathy 67 0.146
162
P RTN016 Retinal Degeneration 52 0.146
163
P BCL017 B-Cell Lymphoma 57 0.146
164
DFF035 Diffuse Cutaneous Systemic Sclerosis 45 0.146
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