Search results for "[genes] LEP"

78 hits were found for '[genes] LEP'

# Family MCID Name MIFTS Score
1
P OBS005 Obesity 93 19.487
2
BLM002 Bulimia Nervosa 54 15.911
3
P PLY011 Polycystic Ovary Syndrome 66 14.525
4
P HYP060 Hyperinsulinism 59 14.525
5
MRB003 Morbid Obesity 58 14.525
6
GST033 Gestational Diabetes 56 14.525
7
GLC003 Glucose Intolerance 55 14.525
8
OBS063 Obesity, Morbid, Due to Leptin Deficiency 24 14.525
9
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 12.991
10
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 12.991
11
P LVR013 Liver Disease 72 12.991
12
c CHR089 Chronic Kidney Failure 66 12.991
13
OBS061 Obstructive Sleep Apnea 66 12.991
14
P ANR007 Anorexia Nervosa 63 12.991
15
P PRD006 Prader-Willi Syndrome 63 12.991
16
P NRC002 Narcolepsy 62 12.991
17
HYP066 Hyperglycemia 60 12.991
18
FTT001 Fatty Liver Disease 60 12.991
19
ETN001 Eating Disorder 60 12.991
20
P MSC007 Muscle Hypertrophy 59 12.991
21
ACN002 Acanthosis Nigricans 57 12.991
22
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 56 12.991
23
P HYP076 Hyperthyroidism 56 12.991
24
P LPD010 Lipodystrophy 52 12.991
25
MYM001 Myoma 51 12.991
26
P FML012 Familial Partial Lipodystrophy 51 12.991
27
URM002 Uremia 50 12.991
28
PRT038 Protein-Energy Malnutrition 49 12.991
29
c SVR005 Severe Pre-Eclampsia 48 12.991
30
NTR005 Nutritional Deficiency Disease 39 12.991
31
P AST005 Asthma 82 11.251
32
P OST002 Osteoporosis 64 11.251
33
P SLP006 Sleep Apnea 61 11.251
34
LPD008 Lipid Metabolism Disorder 58 11.251
35
P PRC031 Preeclampsia/eclampsia 1 57 11.251
36
NNL002 Nonalcoholic Steatohepatitis 53 11.251
37
AMN001 Amenorrhea 51 11.251
38
PLC005 Placental Insufficiency 50 11.251
39
OVR063 Overnutrition 49 11.251
40
ADR013 Adrenal Gland Hyperfunction 47 11.251
41
PRM003 Premature Ejaculation 46 11.251
42
ANV001 Anovulation 45 11.251
43
c CNG012 Congenital Generalized Lipodystrophy 45 11.251
44
IDP070 Idiopathic Scoliosis 40 11.251
45
PLC006 Placental Choriocarcinoma 32 11.251
46
CNG376 Congenital Leptin Deficiency 16 11.251
47
c HYP595 Hypertension, Essential 69 9.186
48
P BRD002 Bardet-Biedl Syndrome 62 9.186
49
P HYP055 Hypoplastic Left Heart Syndrome 60 9.186
50
P KLL001 Kallmann Syndrome 60 9.186
51
PLM031 Poliomyelitis 59 9.186
52
PNC034 Pancreas Disease 57 9.186
53
P AVS004 Avascular Necrosis of the Femoral Head 56 9.186
54
c CNT075 Central Precocious Puberty 53 9.186
55
SLP005 Sleep Disorder 53 9.186
56
END030 End Stage Renal Failure 52 9.186
57
ALS001 Alstrom Syndrome 52 9.186
58
c LPD037 Lipodystrophy, Familial Partial, 2 51 9.186
59
GLC008 Glucose Metabolism Disease 47 9.186
60
P CRN074 Coronary Artery Aneurysm 44 9.186
61
c CNT015 Central Sleep Apnea 44 9.186
62
PRD004 Prediabetes Syndrome 43 9.186
63
END038 Endocrine Pancreas Disease 43 9.186
64
NNT049 Nontuberculous Mycobacterial Lung Disease 41 9.186
65
FTL021 Fetal Macrosomia 41 9.186
66
P ACQ009 Acquired Metabolic Disease 41 9.186
67
P ACQ022 Acquired Generalized Lipodystrophy 40 9.186
68
SCK001 Sick Building Syndrome 39 9.186
69
MLT002 Multiple Symmetrical Lipomatosis 36 9.186
70
LTR003 Lateral Medullary Syndrome 35 9.186
71
LPB001 Lipoblastoma 35 9.186
72
MLD002 Mild Pre-Eclampsia 34 9.186
73
BRR012 Berardinelli-Seip Congenital Lipodystrophy 30 9.186
74
IDP041 Idiopathic Recurrent Pericarditis 30 9.186
75
GST038 Gastrointestinal Adenoma 29 9.186
76
CLS040 Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 27 9.186
77
INS024 Insulin-Like Growth Factor I 74 6.496
78
OBS050 Obesity Due to Congenital Leptin Deficiency 7 6.496