Search results for gdf3

87 hits were found for gdf3

# Family MCID Name MIFTS Score
1
c KLP006 Klippel-Feil Syndrome 3, Autosomal Dominant 20 34.821
2
c MCR108 Microphthalmia, Isolated 7 18 33.303
3
P MCR352 Microphthalmia, Isolated, with Coloboma 6 30 32.893
4
MCR013 Microphthalmia 60 32.138
5
ISL096 Isolated Klippel-Feil Syndrome 34 22.611
6
CLB026 Colobomatous Microphthalmia 46 18.721
7
EMB004 Embryonal Carcinoma 56 18.373
8
P SCL018 Scoliosis 57 17.664
9
P KLP003 Klippel-Feil Syndrome 47 17.300
10
TRT001 Teratocarcinoma 42 13.071
11
c KLP013 Klippel-Feil Syndrome 3 6 11.784
12
CLB010 Coloboma of Macula 53 10.692
13
P SYR001 Syringomyelia 47 8.607
14
SPN221 Spina Bifida Occulta 40 7.688
15
CHL049 Childhood Endodermal Sinus Tumor 19 7.688
16
TST017 Testicular Malignant Germ Cell Cancer 16 7.688
17
GRM001 Germ Cell and Embryonal Cancer 25 7.688
18
SMN007 Seminoma 42 3.109
19
P TRT010 Teratoma 51 2.801
20
GRM010 Germ Cells Tumors 33 2.646
21
TXC005 Toxic Shock Syndrome 62 2.584
22
P TST021 Testicular Germ Cell Tumor 61 2.507
23
P VNT002 Ventricular Septal Defect 58 2.465
24
HRT011 Heart Septal Defect 49 2.465
25
FRY006 Fryns Microphthalmia Syndrome 52 2.337
26
STS002 Situs Inversus 45 2.199
27
DXT002 Dextrocardia with Situs Inversus 43 2.199
28
AGN016 Aging 54 2.045
29
CHR074 Choriocarcinoma 46 2.045
30
TST018 Testicular Yolk Sac Tumor 39 2.045
31
P END039 Endodermal Sinus Tumor 41 2.045
32
P CLB034 Coloboma, Ocular, Autosomal Dominant 49 1.871
33
c LBR029 Leber Congenital Amaurosis 17 35 1.871
34
LBR036 Leber Plus Disease 66 1.871
35
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.300
36
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.300
37
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.300
38
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 1.300
39
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.300
40
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 1.300
41
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.300
42
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 1.300
43
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.300
44
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.300
45
P END044 Endometriosis 62 1.126
46
SVR004 Severe Combined Immunodeficiency 72 1.126
47
SYR010 Syringomyelia, Noncommunicating Isolated 36 0.919
48
DWN001 Down Syndrome 70 0.919
49
c MNS008 Monosomy 21 25 0.919
50
HTR003 Heterotaxy 43 0.919
51
CHR178 Chromosomal Triplication 34 0.919
52
P BRS047 Breast Cancer 98 0.851
53
SNG003 Single Ventricular Heart 30 0.650
54
P OVR082 Overgrowth Syndrome 49 0.650
55
c MCR263 Microphthalmia, Syndromic 1 48 0.650
56
P SCH015 Schizophrenia 74 0.650
57
HLC007 Helicobacter Pylori Infection 67 0.650
58
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.650
59
SPR031 Sprengel Deformity 28 0.650
60
c KLP008 Klippel-Feil Syndrome 2, Autosomal Recessive 28 0.650
61
P RTN024 Retinoblastoma 73 0.650
62
PTR032 Peters-Plus Syndrome 63 0.650
63
DGR001 Digeorge Syndrome 62 0.650
64
c MCR252 Microphthalmia, Syndromic 5 38 0.650
65
LMY002 Leiomyoma 51 0.650
66
DGN001 Degenerative Disc Disease 49 0.650
67
P CTR002 Cataract 60 0.650
68
ALL029 Allergic Disease 59 0.650
69
TST014 Testicular Cancer 52 0.650
70
PRM013 Premature Menopause 58 0.650
71
P INF032 Infertility 57 0.650
72
P EYD002 Eye Disease 57 0.650
73
LRY017 Laryngeal Disease 45 0.650
74
P INS002 in Situ Carcinoma 53 0.650
75
1Q2003 1q21.1 Recurrent Microdeletion 22 0.650
76
P HYP055 Hypoplastic Left Heart Syndrome 65 0.650
77
SX2004 Sox2 Disorder 13 0.650
78
ASH001 Asherman's Syndrome 33 0.650
79
P PNC035 Pancreatic Cancer 86 0.602
80
c GLM047 Glioma Susceptibility 3 33 0.464
81
c MSM022 Mismatch Repair Cancer Syndrome 1 70 0.464
82
c GLM025 Glioma Susceptibility 2 30 0.464
83
c GLM043 Glioma Susceptibility 9 30 0.464
84
P GLM040 Glioma Susceptibility 1 71 0.464
85
MNN043 Meningioma, Familial 79 0.464
86
P OLG002 Oligodendroglioma 66 0.464
87
GLM045 Glioma 63 0.464
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