Search results for myo1d

64 hits were found for myo1d

# Family MCID Name MIFTS Score
1
RFR003 Refractive Error 41 12.931
2
P VSC013 Visceral Heterotaxy 53 9.144
3
CNV004 Canavan Disease 61 9.144
4
P PRC031 Preeclampsia/eclampsia 1 43 1.774
5
c PRC016 Pre-Eclampsia 64 1.774
6
CLT003 Colitis 63 1.364
7
STS002 Situs Inversus 44 1.148
8
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 59 0.836
9
c CLR087 Colorectal Cancer 12 34 0.836
10
GST103 Gastric Cancer, Hereditary Diffuse 68 0.836
11
CLN015 Colon Adenocarcinoma 64 0.836
12
SML009 Small Intestine Adenocarcinoma 57 0.836
13
P BRS047 Breast Cancer 97 0.811
14
c MSM022 Mismatch Repair Cancer Syndrome 1 69 0.724
15
c GLM043 Glioma Susceptibility 9 30 0.724
16
c GLM025 Glioma Susceptibility 2 30 0.724
17
c GLM047 Glioma Susceptibility 3 32 0.724
18
MNN043 Meningioma, Familial 79 0.724
19
P GLM040 Glioma Susceptibility 1 70 0.724
20
P OLG002 Oligodendroglioma 66 0.724
21
GLM045 Glioma 62 0.724
22
P GST053 Gastric Cancer 82 0.573
23
P PNC035 Pancreatic Cancer 87 0.573
24
P FML011 Familial Adenomatous Polyposis 70 0.526
25
c RTN172 Retinitis Pigmentosa 1 45 0.304
26
P PTN014 Patent Ductus Arteriosus 1 59 0.304
27
P RTN008 Retinitis Pigmentosa 79 0.304
28
NRR001 Neuroretinitis 42 0.304
29
RTN023 Retinitis 45 0.304
30
c ATS007 Autism Spectrum Disorder 71 0.248
31
BNR002 Bone Resorption Disease 47 0.248
32
RTN017 Retinal Detachment 60 0.175
33
P ATS364 Autism 72 0.175
34
ALS001 Alstrom Syndrome 65 0.175
35
P PRS040 Prostate Cancer 95 0.175
36
P PRD006 Prader-Willi Syndrome 60 0.175
37
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.175
38
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.175
39
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.175
40
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.175
41
ATS010 Autosomal Recessive Disease 42 0.175
42
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.175
43
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.175
44
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.175
45
KNB006 Knobloch Syndrome 1 44 0.175
46
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.175
47
c ATS371 Autism 6 21 0.175
48
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.175
49
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.175
50
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.175
51
P HPT023 Hepatocellular Carcinoma 95 0.175
52
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.175
53
c NPH031 Nephronophthisis 3 46 0.175
54
MTR002 Mitral Valve Insufficiency 51 0.175
55
P MYP006 Myopia 55 0.175
56
P HYP040 Hypospadias 51 0.175
57
P NRF002 Neurofibromatosis 60 0.175
58
P PLM034 Pulmonary Emphysema 58 0.175
59
P ENC008 Encephalocele 46 0.175
60
P VTR008 Vitreoretinal Degeneration 30 0.175
61
P KNB001 Knobloch Syndrome 37 0.175
62
CRB086 Cerebral Aneurysms 40 0.175
63
OCC011 Occipital Encephalocele 27 0.175
64
GNT167 Genetic Obesity 33 0.175
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