Search results for Mecasermin

259 hits were found for Mecasermin

# Family MCID Name MIFTS Score
1
INS024 Insulin-Like Growth Factor I 79 0.140
2
ACD008 Acid-Labile Subunit Deficiency 54 0.123
3
LRN002 Laron Syndrome 63 0.095
4
P RTT002 Rett Syndrome 80 0.087
5
HYP056 Hypoglycemia 66 0.087
6
DWR001 Dwarfism 44 0.087
7
P THR117 Three M Syndrome 1 63 0.078
8
ISL014 Isolated Growth Hormone Deficiency, Type Ia 55 0.078
9
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.067
10
P HRT032 Heart Disease 75 0.067
11
P MYC007 Myocardial Infarction 70 0.067
12
CNG034 Congestive Heart Failure 70 0.067
13
P MSC005 Muscular Dystrophy 66 0.067
14
ANR007 Anorexia Nervosa 63 0.067
15
c ACT075 Acute Myocardial Infarction 56 0.067
16
P LTR001 Lateral Sclerosis 53 0.067
17
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.055
18
SVR004 Severe Combined Immunodeficiency 73 0.055
19
P OST002 Osteoporosis 73 0.055
20
c EXD008 Exudative Vitreoretinopathy 1 69 0.055
21
c ATS007 Autism Spectrum Disorder 67 0.055
22
SVR066 Severe Combined Immunodeficiency, X-Linked 65 0.055
23
P ATS364 Autism 65 0.055
24
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.055
25
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 61 0.055
26
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.055
27
P SCL018 Scoliosis 60 0.055
28
P EHL001 Ehlers-Danlos Syndrome 57 0.055
29
CMB003 Combined T Cell and B Cell Immunodeficiency 52 0.055
30
P MSC003 Muscular Atrophy 52 0.055
31
P MYT002 Myotonic Dystrophy 49 0.055
32
GRW007 Growth Hormone Deficiency 43 0.055
33
GRW003 Growth Hormone Insensitivity with Immunodeficiency 28 0.055
34
P HPT023 Hepatocellular Carcinoma 100 0.039
35
P CLR023 Colorectal Cancer 98 0.039
36
P LNG032 Lung Cancer 97 0.039
37
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.039
38
MYL069 Myeloma, Multiple 85 0.039
39
P PNC035 Pancreatic Cancer 84 0.039
40
c HYP595 Hypertension, Essential 84 0.039
41
c LKM061 Leukemia, Acute Myeloid 83 0.039
42
P ATX030 Ataxia-Telangiectasia 83 0.039
43
P GLM040 Glioma Susceptibility 1 81 0.039
44
CYS001 Cystic Fibrosis 80 0.039
45
P RHM011 Rheumatoid Arthritis 80 0.039
46
STR067 Stroke, Ischemic 80 0.039
47
OST012 Osteoarthritis 78 0.039
48
IMM167 Immune Deficiency Disease 78 0.039
49
P NNN008 Noonan Syndrome 1 76 0.039
50
P PRK057 Parkinson Disease, Late-Onset 76 0.039
51
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.039
52
DFC004 Deficiency Anemia 75 0.039
53
CRH001 Crohn's Disease 74 0.039
54
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.039
55
ACR006 Aceruloplasminemia 73 0.039
56
LPT014 Leptin Deficiency or Dysfunction 73 0.039
57
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.039
58
P MLT020 Multiple Sclerosis 72 0.039
59
MSC157 Muscular Dystrophy, Duchenne Type 71 0.039
60
PRP027 Peripheral Vascular Disease 71 0.039
61
ACR007 Acromegaly 71 0.039
62
P KDN018 Kidney Disease 70 0.039
63
DWN001 Down Syndrome 70 0.039
64
P ART022 Arthritis 70 0.039
65
MYL009 Myelodysplastic Syndrome 70 0.039
66
ADL002 Adult Syndrome 69 0.039
67
RCK004 Rickets 69 0.039
68
WRN001 Werner Syndrome 69 0.039
69
CRB039 Cerebrovascular Disease 69 0.039
70
P HYP086 Hypothyroidism 68 0.039
71
EWN003 Ewing Sarcoma 68 0.039
72
P PLM037 Pulmonary Hypertension 68 0.039
73
c INF071 Inflammatory Bowel Disease 1 68 0.039
74
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.039
75
P HPT021 Hepatitis 67 0.039
76
P DMN002 Dementia 67 0.039
77
P SKN015 Skin Carcinoma 67 0.039
78
P LKM002 Leukemia 66 0.039
79
OST159 Osteogenic Sarcoma 66 0.039
80
FCT007 Factor Vii Deficiency 66 0.039
81
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.039
82
c MYT021 Myotonic Dystrophy 1 66 0.039
83
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.039
84
MYX005 Myxoid Liposarcoma 66 0.039
85
ATH013 Atherosclerosis Susceptibility 66 0.039
86
SRC014 Sarcoma 65 0.039
87
c SML038 Small Cell Cancer of the Lung 65 0.039
88
c RHB024 Rhabdomyosarcoma 2 65 0.039
89
P LPS002 Liposarcoma 65 0.039
90
MSM014 Mismatch Repair Cancer Syndrome 65 0.039
91
P TRN020 Turner Syndrome 65 0.039
92
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.039
93
P BRL012 Bare Lymphocyte Syndrome, Type Ii 65 0.039
94
P DBT009 Diabetes Mellitus 64 0.039
95
P MTR014 Motor Neuron Disease 64 0.039
96
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.039
97
ALL026 Allergic Hypersensitivity Disease 64 0.039
98
P ADN016 Adenocarcinoma 64 0.039
99
KHL003 Kohlschutter-Tonz Syndrome 64 0.039
100
P VSC007 Vascular Disease 63 0.039
101
MSC007 Muscle Hypertrophy 63 0.039
102
c PRC016 Pre-Eclampsia 63 0.039
103
DPR016 Depression 63 0.039
104
P CRN018 Coronary Artery Anomaly 63 0.039
105
P GLM045 Glioma 63 0.039
106
P CRN300 Coronary Heart Disease 1 63 0.039
107
SKN016 Skin Disease 63 0.039
108
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.039
109
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.039
110
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.039
111
P RHB003 Rhabdomyosarcoma 62 0.039
112
P ART023 Arthropathy 62 0.039
113
HSH003 Hashimoto Thyroiditis 62 0.039
114
DNH001 Donohue Syndrome 62 0.039
115
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.039
116
NTR005 Nutritional Deficiency Disease 61 0.039
117
INT002 Intermittent Claudication 61 0.039
118
FTT001 Fatty Liver Disease 61 0.039
119
HYP066 Hyperglycemia 61 0.039
120
P HYP097 Hyperekplexia 61 0.039
121
ALV005 Alveolar Soft Part Sarcoma 61 0.039
122
LNG099 Lung Disease 61 0.039
123
PHL006 Phelan-Mcdermid Syndrome 61 0.039
124
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.039
125
P ALP009 Alopecia Areata 60 0.039
126
ORL011 Oral Cancer 60 0.039
127
ETN001 Eating Disorder 59 0.039
128
P BND020 Bone Disease 59 0.039
129
P CHR285 Chronic Myelomonocytic Leukemia 59 0.039
130
FBR047 Fibromyalgia 59 0.039
131
ADN018 Adenoma 58 0.039
132
PRL032 Perlman Syndrome 58 0.039
133
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.039
134
EYD002 Eye Disease 58 0.039
135
ADR005 Adrenal Carcinoma 58 0.039
136
P PRV006 Pervasive Developmental Disorder 57 0.039
137
BLM002 Bulimia Nervosa 57 0.039
138
P HDC001 Headache 57 0.039
139
GST033 Gestational Diabetes 57 0.039
140
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.039
141
BRN056 Bronchopulmonary Dysplasia 57 0.039
142
c MST023 Mesothelioma, Malignant 57 0.039
143
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.039
144
MNT002 Mental Depression 57 0.039
145
P DRR001 Diarrhea 57 0.039
146
SRC027 Sarcoma, Synovial 56 0.039
147
P CHN012 Chondrosarcoma 56 0.039
148
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 56 0.039
149
SFT003 Soft Tissue Sarcoma 56 0.039
150
P ALP008 Alopecia 56 0.039
151
P CRD246 Cardiovascular System Disease 56 0.039
152
AGN016 Aging 56 0.039
153
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 56 0.039
154
P INF037 Inflammatory Bowel Disease 56 0.039
155
MCL006 Macular Retinal Edema 55 0.039
156
P GRV001 Graves' Disease 55 0.039
157
c GRV008 Graves Disease 1 55 0.039
158
P HYP076 Hyperthyroidism 55 0.039
159
HYP060 Hyperinsulinism 54 0.039
160
P LCH002 Lichen Planus 54 0.039
161
CRT017 Cartilage Disease 54 0.039
162
ANL018 Analbuminemia 54 0.039
163
GLC003 Glucose Intolerance 54 0.039
164
PTT009 Pituitary Gland Disease 54 0.039
165
INT075 Intracranial Hypertension 53 0.039
166
TRM010 Traumatic Brain Injury 53 0.039
167
P HYP083 Hypopituitarism 53 0.039
168
GST023 Gastric Ulcer 53 0.039
169
P EMB005 Embryonal Rhabdomyosarcoma 53 0.039
170
P THY032 Thyroiditis 53 0.039
171
P RTN018 Retinal Disease 52 0.039
172
CRH005 Crohn's Colitis 52 0.039
173
EXP004 Exophthalmos 52 0.039
174
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.039
175
ACR041 Acromelic Frontonasal Dysostosis 52 0.039
176
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.039
177
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 52 0.039
178
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.039
179
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 52 0.039
180
TND005 Tendinitis 52 0.039
181
c GLL024 Gallbladder Disease 1 52 0.039
182
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.039
183
ISL003 Isolated Growth Hormone Deficiency 52 0.039
184
OCL069 Ocular Motor Apraxia 51 0.039
185
PLS009 Plasma Cell Neoplasm 51 0.039
186
TLN003 Telangiectasis 51 0.039
187
NNL006 Non-Alcoholic Steatohepatitis 51 0.039
188
THY030 Thyroid Gland Disease 51 0.039
189
SPN035 Spindle Cell Sarcoma 51 0.039
190
HYP081 Hypolipoproteinemia 50 0.039
191
LNG031 Lung Benign Neoplasm 50 0.039
192
HYP080 Hypogonadism 50 0.039
193
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.039
194
P OVR082 Overgrowth Syndrome 50 0.039
195
c HYP699 Hyperekplexia 1 50 0.039
196
BRN071 Brain Injury 49 0.039
197
c INF023 Inflammatory Breast Carcinoma 49 0.039
198
PLC008 Placenta Disease 49 0.039
199
c LRG001 Large Cell Carcinoma 49 0.039
200
ADN009 Adenosquamous Carcinoma 49 0.039
201
RFR010 Refractory Anemia 48 0.039
202
DBT006 Diabetic Macular Edema 48 0.039
203
RTN020 Retinal Vascular Disease 48 0.039
204
ATX019 Ataxia with Vitamin E Deficiency 48 0.039
205
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.039
206
CMB081 Combined Immunodeficiency, X-Linked 48 0.039
207
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.039
208
ADR016 Adrenal Cortical Carcinoma 48 0.039
209
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.039
210
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.039
211
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.039
212
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.039
213
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.039
214
KRT013 Keratolytic Winter Erythema 46 0.039
215
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.039
216
GLL048 Glial Tumor 45 0.039
217
c MLG068 Malignant Glioma 45 0.039
218
MXD026 Mixed Glioma 45 0.039
219
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.039
220
P BNG032 Benign Mesothelioma 45 0.039
221
ORL013 Oral Lichen Planus 45 0.039
222
PPL001 Papillary Adenoma 45 0.039
223
PTT037 Pituitary Tumors 44 0.039
224
TND004 Tendinopathy 44 0.039
225
c CLR017 Clear Cell Sarcoma 44 0.039
226
CYT002 Cytokine Deficiency 44 0.039
227
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.039
228
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.039
229
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.039
230
BRN032 Brain Glioma 43 0.039
231
c RHB023 Rhabdomyosarcoma, Embryonal, 1 43 0.039
232
CHN056 Chondrosarcoma, Extraskeletal Myxoid 43 0.039
233
c PRM038 Primary Agammaglobulinemia 43 0.039
234
ORL015 Oral Squamous Cell Carcinoma 43 0.039
235
MYF002 Myofascial Pain Syndrome 42 0.039
236
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.039
237
P HYP265 Hypotonia 42 0.039
238
FTL021 Fetal Macrosomia 42 0.039
239
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.039
240
MMM006 Mammographic Density 41 0.039
241
HYP064 Hypogonadotropism 40 0.039
242
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.039
243
48X005 48,xyyy 39 0.039
244
MCC013 Mucocutaneous Ulceration, Chronic 39 0.039
245
c MLG074 Malignant Mesenchymoma 39 0.039
246
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.039
247
ADR004 Adrenal Cortical Adenocarcinoma 38 0.039
248
c ADL096 Adult Hepatocellular Carcinoma 35 0.039
249
P EXT030 Extraosseous Chondrosarcoma 34 0.039
250
P VSC018 Visceral Steatosis 33 0.039
251
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.039
252
P MYX008 Myxoid Chondrosarcoma 32 0.039
253
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.039
254
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.039
255
CHL079 Children's Interstitial Lung Disease 27 0.039
256
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.039
257
c CHR464 Chronic Intestinal Failure 23 0.039
258
LYM053 Lymphomatous Thyroiditis 22 0.039
259
c PSD047 Pseudo-Turner Syndrome 21 0.039
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