Search results for INSR

107 hits were found for INSR

# Family MCID Name MIFTS Score
1
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 53 15.778
2
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 57 14.277
3
DBT020 Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 39 9.226
4
DNH001 Donohue Syndrome 62 7.617
6
P DBT009 Diabetes Mellitus 64 4.234
7
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 4.109
8
ACN002 Acanthosis Nigricans 60 3.936
9
HYP056 Hypoglycemia 66 3.916
10
HYP060 Hyperinsulinism 54 3.916
11
P BRS047 Breast Cancer 97 3.823
12
P ADN016 Adenocarcinoma 64 3.823
13
P PLY011 Polycystic Ovary Syndrome 56 3.720
14
P ALZ034 Alzheimer Disease 88 3.474
15
NNL005 Non-Alcoholic Fatty Liver Disease 61 3.448
16
GLC003 Glucose Intolerance 54 3.448
17
HYP043 Hyperandrogenism 48 3.448
18
P HYP050 Hyperinsulinemic Hypoglycemia 55 3.420
19
HYP066 Hyperglycemia 61 3.049
20
GST033 Gestational Diabetes 61 3.023
21
c HYP595 Hypertension, Essential 84 2.994
22
RNL114 Renal Cell Carcinoma, Nonpapillary 78 2.962
23
P PHC003 Pheochromocytoma 71 2.962
24
P LVR013 Liver Disease 68 2.962
25
FTT001 Fatty Liver Disease 61 2.962
26
P OVR049 Ovarian Disease 52 2.962
27
LPD008 Lipid Metabolism Disorder 62 2.518
28
INS024 Insulin-Like Growth Factor I 79 2.457
29
P MYP004 Myopathy 70 2.457
30
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 2.418
31
P MSC005 Muscular Dystrophy 66 2.418
32
P ATT013 Attention Deficit-Hyperactivity Disorder 65 2.418
33
c DBT099 Diabetes Mellitus, Type I 65 2.418
34
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 2.418
35
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 2.418
36
P MGR003 Migraine with Aura 52 2.418
37
c RRD013 Rare Diabetes Mellitus Type 2 31 1.886
38
FST010 Fasting Hypoglycemia 35 1.760
39
P CNT004 Centronuclear Myopathy 59 1.710
40
PGM003 Pigmentation Disease 46 1.710
41
MYP091 Myopathy, Congenital, with Fiber-Type Disproportion 43 1.710
42
FTL021 Fetal Macrosomia 42 1.710
43
MYT003 Myotonic Disease 35 1.710
44
MNG006 Monogenic Diabetes 46 0.285
45
RRG011 Rare Genetic Diabetes Mellitus 23 0.285
46
ATS010 Autosomal Recessive Disease 48 0.136
47
P OVR042 Ovarian Cancer 88 0.105
48
NPH003 Nephrocalcinosis 51 0.105
49
P GST053 Gastric Cancer 83 0.086
50
c PRC016 Pre-Eclampsia 63 0.086
51
ESP020 Esophageal Atresia 62 0.086
52
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.086
53
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.086
54
P INF032 Infertility 57 0.086
55
P MLN007 Male Infertility 55 0.086
56
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 55 0.086
57
c MCR113 Microvascular Complications of Diabetes 3 52 0.086
58
P HYP077 Hypertrichosis 50 0.086
59
AZS001 Azoospermia 50 0.086
60
P MYT002 Myotonic Dystrophy 49 0.086
61
PYL006 Pyloric Stenosis 48 0.086
62
c MCR120 Microvascular Complications of Diabetes 7 47 0.086
63
c MCR130 Microvascular Complications of Diabetes 6 41 0.086
64
c MCR133 Microvascular Complications of Diabetes 4 41 0.086
65
P CLR023 Colorectal Cancer 99 0.061
66
P PRS040 Prostate Cancer 97 0.061
67
c NRF023 Neurofibromatosis, Type Ii 80 0.061
68
c ATR087 Atrial Standstill 1 75 0.061
69
END057 Endometrial Cancer 74 0.061
70
LPT014 Leptin Deficiency or Dysfunction 74 0.061
71
c SPN225 Spondyloarthropathy 1 73 0.061
72
GST040 Gastric Adenocarcinoma 70 0.061
73
P ANG001 Angelman Syndrome 69 0.061
74
P LKM062 Leukemia, Acute Lymphoblastic 69 0.061
75
P HPT021 Hepatitis 67 0.061
76
c MGR028 Migraine with or Without Aura 1 67 0.061
77
P CCK001 Cockayne Syndrome 66 0.061
78
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.061
79
P MTR004 Maturity-Onset Diabetes of the Young 65 0.061
80
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.061
81
INC021 Incontinentia Pigmenti 63 0.061
82
P ANR048 Aniridia 1 63 0.061
83
ANR007 Anorexia Nervosa 63 0.061
84
P TRC086 Trichohepatoenteric Syndrome 1 62 0.061
85
P PLY006 Polydactyly 59 0.061
86
P BCL017 B-Cell Lymphoma 58 0.061
87
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.061
88
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.061
89
THR013 Thoracic Outlet Syndrome 54 0.061
90
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.061
91
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.061
92
SCH012 Schizoaffective Disorder 50 0.061
93
P OVR082 Overgrowth Syndrome 50 0.061
94
P ECL001 Eclampsia 50 0.061
95
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.061
96
OLG001 Oligospermia 45 0.061
97
P HYP265 Hypotonia 43 0.061
98
ICH020 Ichthyosis Prematurity Syndrome 40 0.061
99
OVR094 Ovarian Epithelial Cancer 38 0.061
100
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.061
101
c JVN002 Juvenile Type Testicular Granulosa Cell Tumor 35 0.061
102
c NRP064 Neuropathy, Congenital Hypomyelinating, 2 35 0.061
103
ATX010 Ataxia Neuropathy Spectrum 34 0.061
104
GRN022 Granulosa Cell Tumor of the Ovary 34 0.061
105
ACT064 Acute Necrotizing Encephalitis 33 0.061
106
c NLD006 Nail Disorder, Nonsyndromic Congenital, 9 31 0.061
107
BLD137 Blood Group--Ahonen 16 0.061
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