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Search results for lgr4

118 hits were found for lgr4

# Family MCID Name MIFTS Score
1
c BNM031 Bone Mineral Density Quantitative Trait Locus 17 15 28.547
2
P ANT088 Anterior Segment Dysgenesis 55 15.741
3
P OST002 Osteoporosis 76 14.034
4
NRR002 Norrie Disease 61 10.330
5
WLM014 Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome 52 10.330
6
BLR013 Biliary Tract Cancer 43 10.025
7
P EXD001 Exudative Vitreoretinopathy 56 9.179
8
EXP002 Exposure Keratitis 26 8.324
9
RPD005 Rapidly Involuting Congenital Hemangioma 46 7.624
10
P PRS040 Prostate Cancer 95 5.239
11
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 4.389
12
BNR002 Bone Resorption Disease 47 3.837
13
c PCH010 Pachyonychia Congenita 3 43 3.490
14
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 3.472
15
P CTR002 Cataract 60 2.930
16
OST012 Osteoarthritis 77 2.834
17
c THY109 Thyroid Cancer, Nonmedullary, 1 55 2.749
18
THY029 Thyroid Carcinoma 51 2.749
19
CRD016 Cardiac Rupture 34 2.749
20
SQM006 Squamous Cell Carcinoma 60 2.739
21
HYP266 Hypoxia 57 2.739
22
P MLN069 Melanoma, Uveal 61 2.660
23
P MLN008 Melanoma 76 2.660
24
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 2.468
25
P GST053 Gastric Cancer 83 2.468
26
DPR016 Depression 65 2.468
27
P VTR007 Vitreoretinopathy 46 2.364
28
TNG009 Tongue Squamous Cell Carcinoma 43 2.277
29
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 2.262
30
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 2.262
31
P OVR042 Ovarian Cancer 88 2.254
32
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 2.254
33
P INF037 Inflammatory Bowel Disease 53 2.254
34
RNL025 Renal Hypoplasia 41 2.254
35
MYL069 Myeloma, Multiple 77 2.254
36
MCR013 Microphthalmia 60 2.254
37
c MCR115 Microvascular Complications of Diabetes 5 65 2.135
38
P PLY014 Polycystic Kidney Disease 69 2.135
39
P MCR129 Microvascular Complications of Diabetes 1 68 2.135
40
INT323 Intraocular Pressure Quantitative Trait Locus 64 2.135
41
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 2.135
42
P RTN024 Retinoblastoma 73 2.135
43
GLL048 Glial Tumor 52 2.135
44
c MCR112 Microvascular Complications of Diabetes 2 42 2.135
45
P AXN002 Axenfeld-Rieger Syndrome 63 2.135
46
GLM045 Glioma 63 2.135
47
AML065 Amelia 29 2.006
48
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.006
49
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.006
50
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.006
51
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 2.006
52
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 2.006
53
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 2.006
54
c TTR029 Tetraamelia Syndrome 2 24 2.006
55
HMR045 Humerofemoral Hypoplasia with Radiotibial Ray Deficiency 17 2.006
56
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.006
57
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 2.006
58
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.006
59
c TYP009 Type 2 Diabetes Mellitus 92 2.006
60
P ANR048 Aniridia 1 64 2.006
61
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 2.006
62
P TTR031 Tetraamelia Syndrome 35 2.006
63
P MLN007 Male Infertility 56 2.006
64
PPL022 Papilloma 53 2.006
65
SQM002 Squamous Cell Papilloma 46 2.006
66
TXC005 Toxic Shock Syndrome 62 2.006
67
P HRP006 Herpes Simplex 65 2.005
68
RBS001 Rabies 58 2.005
69
NWC001 Newcastle Disease 47 2.005
70
STM007 Stomatitis 54 2.005
71
ATH013 Atherosclerosis Susceptibility 63 1.912
72
PRS129 Prostatic Hyperplasia, Benign 49 1.863
73
PRS021 Prostatic Adenoma 43 1.863
74
PRS045 Prostatic Hypertrophy 53 1.863
75
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.710
76
c CHR684 Chronic Kidney Disease 69 1.710
77
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.701
78
c LKM061 Leukemia, Acute Myeloid 83 1.701
79
P MYL006 Myeloid Leukemia 61 1.701
80
P ALP008 Alopecia 54 1.701
81
P LKM002 Leukemia 67 1.701
82
P ECT006 Ectodermal Dysplasia 63 1.701
83
48X005 48,xyyy 39 1.701
84
P CLR023 Colorectal Cancer 100 1.352
85
OST159 Osteogenic Sarcoma 66 1.352
86
SMT018 Smith-Mccort Dysplasia 2 34 0.855
87
c SML038 Small Cell Cancer of the Lung 69 0.855
88
HYP066 Hyperglycemia 61 0.855
89
SKN022 Skin Squamous Cell Carcinoma 54 0.855
90
MST005 Mastitis 53 0.855
91
P BRS047 Breast Cancer 98 0.642
92
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.605
93
CHR100 Chronic Ulcer of Skin 57 0.605
94
P FML011 Familial Adenomatous Polyposis 71 0.605
95
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.605
96
TTH030 Teeth, Supernumerary 33 0.605
97
c EXS019 Exostoses, Multiple, Type I 54 0.605
98
MNN043 Meningioma, Familial 79 0.605
99
RNL077 Renal Fibrosis 46 0.605
100
ORL015 Oral Squamous Cell Carcinoma 43 0.605
101
SVR001 Severe Acute Respiratory Syndrome 67 0.605
102
SCR001 Secretory Meningioma 40 0.605
103
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.605
104
SBC011 Sebaceous Adenocarcinoma 43 0.605
105
P LNG064 Lung Cancer Susceptibility 3 70 0.605
106
c BSL007 Basal Cell Carcinoma 68 0.605
107
P ADN016 Adenocarcinoma 63 0.605
108
SVR004 Severe Combined Immunodeficiency 72 0.605
109
P PSD003 Pseudohypoaldosteronism 44 0.605
110
P INF032 Infertility 57 0.605
111
P SLP005 Sleep Disorder 61 0.605
112
P BNG032 Benign Mesothelioma 53 0.605
113
DMY004 Demyelinating Disease 50 0.605
114
SPN021 Spinal Meningioma 50 0.605
115
ORL011 Oral Cancer 60 0.605
116
P PRC019 Precocious Puberty 47 0.605
117
HPT070 Hepatosplenic T-Cell Lymphoma 36 0.430
118
c NRB010 Neuroblastoma 1 59 0.430
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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