Search results for "[genes] LEP"

83 hits were found for '[genes] LEP'

# Family MCID Name MIFTS Score
1
P OBS005 Obesity 87 19.418
2
BLM002 Bulimia Nervosa 48 15.855
3
P LVR013 Liver Disease 60 14.473
4
P PLY011 Polycystic Ovary Syndrome 58 14.473
5
FTT001 Fatty Liver Disease 53 14.473
6
c MTB001 Metabolic Syndrome X 53 14.473
7
MRB003 Morbid Obesity 50 14.473
8
P HYP060 Hyperinsulinism 49 14.473
9
GST033 Gestational Diabetes 47 14.473
10
GLC003 Glucose Intolerance 47 14.473
11
LPT005 Leptin Deficiency 34 14.473
12
P DBT085 Diabetes Mellitus, Insulin-Dependent 77 12.945
13
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 76 12.945
14
P OST002 Osteoporosis 76 12.945
15
P PRD006 Prader-Willi Syndrome 59 12.945
16
c CHR089 Chronic Kidney Failure 58 12.945
17
P ANR007 Anorexia Nervosa 56 12.945
18
HYP066 Hyperglycemia 53 12.945
19
ETN001 Eating Disorder 52 12.945
20
OBS061 Obstructive Sleep Apnea 51 12.945
21
ACN002 Acanthosis Nigricans 50 12.945
22
P HYP076 Hyperthyroidism 49 12.945
23
P FML012 Familial Partial Lipodystrophy 46 12.945
24
P LPD010 Lipodystrophy 43 12.945
25
c SVR005 Severe Pre-Eclampsia 42 12.945
26
MYM001 Myoma 41 12.945
27
NTR005 Nutritional Deficiency Disease 39 12.945
28
P AST005 Asthma 77 11.211
29
P MYC007 Myocardial Infarction 77 11.211
30
PSD002 Pseudotumor Cerebri 49 11.211
31
P SLP006 Sleep Apnea 47 11.211
32
LPD008 Lipid Metabolism Disorder 47 11.211
33
AMN001 Amenorrhea 46 11.211
34
P SHR001 Short Bowel Syndrome 41 11.211
35
PLC005 Placental Insufficiency 41 11.211
36
ADR013 Adrenal Gland Hyperfunction 40 11.211
37
PRM003 Premature Ejaculation 39 11.211
38
ANV001 Anovulation 38 11.211
39
c CNG012 Congenital Generalized Lipodystrophy 37 11.211
40
IDP070 Idiopathic Scoliosis 36 11.211
41
PRT038 Protein-Energy Malnutrition 36 11.211
42
PLC006 Placental Choriocarcinoma 32 11.211
43
OBS063 Obesity, Morbid, Due to Leptin Deficiency 16 11.211
44
CNG376 Congenital Leptin Deficiency 16 11.211
45
INS024 Insulin-Like Growth Factor I 67 9.154
46
P NRC002 Narcolepsy 62 9.154
47
c HYP595 Hypertension, Essential 62 9.154
48
P KLL001 Kallmann Syndrome 58 9.154
49
P BRD002 Bardet-Biedl Syndrome 52 9.154
50
ALS001 Alstrom Syndrome 51 9.154
51
END030 End Stage Renal Failure 50 9.154
52
DBT062 Diabetic Foot Ulcers 50 9.154
53
P AVS004 Avascular Necrosis of the Femoral Head 49 9.154
54
P PRC031 Preeclampsia/eclampsia 1 49 9.154
55
c PRC016 Pre-Eclampsia 48 9.154
56
c LPD037 Lipodystrophy, Familial Partial, 2 48 9.154
57
NNL002 Nonalcoholic Steatohepatitis 45 9.154
58
OVR063 Overnutrition 41 9.154
59
P CRN074 Coronary Artery Aneurysm 40 9.154
60
MSS002 Mass Syndrome 40 9.154
61
SLP005 Sleep Disorder 40 9.154
62
PNC034 Pancreas Disease 39 9.154
63
NNT049 Nontuberculous Mycobacterial Lung Disease 39 9.154
64
MLT002 Multiple Symmetrical Lipomatosis 38 9.154
65
c CNT015 Central Sleep Apnea 37 9.154
66
GLC008 Glucose Metabolism Disease 35 9.154
67
LTR003 Lateral Medullary Syndrome 34 9.154
68
END038 Endocrine Pancreas Disease 33 9.154
69
P ACQ009 Acquired Metabolic Disease 33 9.154
70
ADL086 Adolescent Idiopathic Scoliosis 33 9.154
71
SCK001 Sick Building Syndrome 32 9.154
72
PRD004 Prediabetes Syndrome 31 9.154
73
BRR012 Berardinelli-Seip Congenital Lipodystrophy 30 9.154
74
IDP041 Idiopathic Recurrent Pericarditis 30 9.154
75
FTL021 Fetal Macrosomia 29 9.154
76
MLD002 Mild Pre-Eclampsia 29 9.154
77
P ACQ022 Acquired Generalized Lipodystrophy 26 9.154
78
CLS040 Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 25 9.154
79
GST038 Gastrointestinal Adenoma 19 9.154
80
FML039 Female Reproductive System Disease 35 6.473
81
DSS024 Disease of Anatomical Entity 34 6.473
82
SPC003 Specific Developmental Disorder 30 6.473
83
RPR002 Reproductive System Disease 29 6.473