Search results for Mecasermin

105 hits were found for Mecasermin

# Family MCID Name MIFTS Score
1
INS024 Insulin-Like Growth Factor I 77 5.392
2
LRN002 Laron Syndrome 62 3.753
3
ACD008 Acid-Labile Subunit Deficiency 52 3.595
4
DWR001 Dwarfism 44 3.300
5
P RTT002 Rett Syndrome 79 3.050
6
P ANR048 Aniridia 1 66 3.028
7
P MSC005 Muscular Dystrophy 66 2.463
8
HYP056 Hypoglycemia 65 2.288
9
ANT039 Antisynthetase Syndrome 55 2.223
10
c AMY091 Amyotrophic Lateral Sclerosis 1 87 2.143
11
P LTR001 Lateral Sclerosis 57 2.143
12
P MYT002 Myotonic Dystrophy 51 2.111
13
ANR007 Anorexia Nervosa 59 2.084
14
ISL014 Isolated Growth Hormone Deficiency, Type Ia 54 1.818
15
P THR117 Three M Syndrome 1 64 1.818
16
GRW007 Growth Hormone Deficiency 47 1.702
17
P OST002 Osteoporosis 76 1.522
18
SVR066 Severe Combined Immunodeficiency, X-Linked 65 1.522
19
c EXD008 Exudative Vitreoretinopathy 1 71 1.522
20
CMB007 Combined Immunodeficiency 56 1.522
21
SVR004 Severe Combined Immunodeficiency 70 1.522
22
c ATS007 Autism Spectrum Disorder 71 1.473
23
P MYC007 Myocardial Infarction 69 1.435
24
CNG034 Congestive Heart Failure 69 1.435
25
P HRT032 Heart Disease 84 1.435
26
c ACT075 Acute Myocardial Infarction 55 1.435
27
GRW003 Growth Hormone Insensitivity with Immunodeficiency 16 1.388
28
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 1.164
29
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 1.164
30
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 1.164
31
P EHL001 Ehlers-Danlos Syndrome 57 1.164
32
AND005 Androgen Insensitivity Syndrome, Mild 21 1.164
33
P PLM037 Pulmonary Hypertension 69 1.154
34
INT075 Intracranial Hypertension 52 1.154
35
P MSC003 Muscular Atrophy 52 1.066
36
WRN001 Werner Syndrome 69 1.011
37
DNH001 Donohue Syndrome 60 0.939
38
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 54 0.939
39
ACR007 Acromegaly 70 0.757
40
PHL006 Phelan-Mcdermid Syndrome 61 0.685
41
P MTR014 Motor Neuron Disease 65 0.685
42
P DBT009 Diabetes Mellitus 67 0.685
43
P PRV006 Pervasive Developmental Disorder 52 0.511
44
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.511
45
CRH005 Crohn's Colitis 53 0.511
46
P INF037 Inflammatory Bowel Disease 53 0.511
47
P ATS364 Autism 72 0.511
48
P BRL012 Bare Lymphocyte Syndrome, Type Ii 65 0.511
49
CYS001 Cystic Fibrosis 77 0.511
50
c MYT021 Myotonic Dystrophy 1 67 0.511
51
P NNN008 Noonan Syndrome 1 76 0.511
52
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.511
53
c TYP009 Type 2 Diabetes Mellitus 91 0.511
54
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.511
55
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 56 0.511
56
MSC157 Muscular Dystrophy, Duchenne Type 78 0.511
57
CMB081 Combined Immunodeficiency, X-Linked 39 0.511
58
c INF071 Inflammatory Bowel Disease 1 65 0.511
59
P MLT020 Multiple Sclerosis 79 0.511
60
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.511
61
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.511
62
c TYP008 Type 1 Diabetes Mellitus 77 0.511
63
IMM167 Immune Deficiency Disease 76 0.511
64
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 0.511
65
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.511
66
ADL002 Adult Syndrome 69 0.511
67
c BLD140 Blood Group, I System 47 0.511
68
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 0.511
69
P BND020 Bone Disease 60 0.511
70
ISL003 Isolated Growth Hormone Deficiency 56 0.511
71
HYP060 Hyperinsulinism 53 0.511
72
P TRN020 Turner Syndrome 67 0.511
73
INT002 Intermittent Claudication 61 0.511
74
PRD004 Prediabetes Syndrome 52 0.511
75
GLC003 Glucose Intolerance 53 0.511
76
RCK004 Rickets 64 0.511
77
KRT002 Keratomalacia 54 0.511
78
P RTN018 Retinal Disease 53 0.511
79
NRN002 Neuronitis 31 0.511
80
BRN056 Bronchopulmonary Dysplasia 57 0.511
81
LNG099 Lung Disease 62 0.511
82
CNG092 Congenital Extrahepatic Portosystemic Shunt 24 0.511
83
CRH001 Crohn's Disease 80 0.511
84
48X005 48,xyyy 39 0.511
85
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.511
86
CHL079 Children's Interstitial Lung Disease 25 0.511
87
CHR682 Chronic Bilirubin Encephalopathy 37 0.511
88
c PSD047 Pseudo-Turner Syndrome 52 0.511
89
LPD008 Lipid Metabolism Disorder 61 0.302
90
OVR063 Overnutrition 42 0.246
91
VRL003 Variola Major 43 0.174
92
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.174
93
P FRG001 Fragile X Syndrome 70 0.174
94
TLR001 Tularemia 56 0.174
95
VCC001 Vaccinia 49 0.174
96
MTR007 Motor Peripheral Neuropathy 41 0.174
97
P MVM001 Movement Disease 61 0.174
98
INF021 Infant Gynecomastia 30 0.174
99
P PTT006 Pituitary Adenoma 55 0.174
100
VGN019 Vaginal Discharge 33 0.174
101
BLL003 Bell's Palsy 48 0.174
102
HYP066 Hyperglycemia 60 0.174
103
GYN001 Gynecomastia 48 0.174
104
ACH005 Achalasia 54 0.174
105
SML019 Smallpox 55 0.174
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