Search results for gapdh

229 hits were found for gapdh

# Family MCID Name MIFTS Score
1
GLY022 Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency 6 3.347
2
P CLR023 Colorectal Cancer 99 3.108
3
P BRS047 Breast Cancer 97 3.040
4
P ALZ034 Alzheimer Disease 88 2.905
5
P HNT016 Huntington Disease 72 2.577
6
P HPT023 Hepatocellular Carcinoma 100 2.543
7
P PRS040 Prostate Cancer 97 2.543
8
P PNC035 Pancreatic Cancer 84 2.525
9
P OVR042 Ovarian Cancer 88 2.505
10
MLR004 Malaria 81 2.505
11
P BLD134 Bladder Cancer 79 2.505
12
P LNG032 Lung Cancer 98 2.482
13
P HRT032 Heart Disease 75 2.482
14
AST005 Asthma 76 2.175
15
P DBT009 Diabetes Mellitus 64 2.175
16
DNT005 Dentatorubral-Pallidoluysian Atrophy 54 2.175
17
c DLT002 Dilated Cardiomyopathy 79 2.150
18
P SCH015 Schizophrenia 74 2.150
19
LVR012 Liver Cirrhosis 62 2.150
20
THY122 Thyroid Gland Cancer 57 2.150
21
SCH014 Schistosomiasis 57 2.150
22
P NRB001 Neuroblastoma 72 1.871
23
CRV035 Cervical Cancer 76 1.833
24
P MYC007 Myocardial Infarction 70 1.811
25
PNC129 Pancreatic Adenocarcinoma 68 1.811
26
c AMY091 Amyotrophic Lateral Sclerosis 1 89 1.785
27
P LNG064 Lung Cancer Susceptibility 3 78 1.785
28
P PRK057 Parkinson Disease, Late-Onset 78 1.785
29
P INF037 Inflammatory Bowel Disease 54 1.785
30
SLP001 Sleeping Sickness 54 1.785
31
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 1.785
32
P MSC003 Muscular Atrophy 52 1.785
34
c HYP595 Hypertension, Essential 84 1.755
35
c NRF023 Neurofibromatosis, Type Ii 80 1.755
36
P RTN008 Retinitis Pigmentosa 79 1.755
37
IMM167 Immune Deficiency Disease 78 1.755
38
RNL114 Renal Cell Carcinoma, Nonpapillary 78 1.755
39
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 1.755
40
P NNN008 Noonan Syndrome 1 76 1.755
41
P CNR004 Cone-Rod Dystrophy 2 73 1.755
42
c LKM063 Leukemia, Chronic Myeloid 72 1.755
43
MNT001 Mantle Cell Lymphoma 69 1.755
44
P MYC084 Mycobacterium Tuberculosis 1 68 1.755
45
P MTR004 Maturity-Onset Diabetes of the Young 65 1.755
46
P THY023 Thymoma 65 1.755
47
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 1.755
48
c DPH024 Diaphragmatic Hernia, Congenital 63 1.755
49
P VSC007 Vascular Disease 63 1.755
50
INT323 Intraocular Pressure Quantitative Trait Locus 62 1.755
51
P OST009 Osteochondritis Dissecans 62 1.755
52
P BNC003 Bone Cancer 58 1.755
53
P END033 Endocarditis 57 1.755
54
ALC009 Alcoholic Liver Cirrhosis 53 1.755
55
P OVR049 Ovarian Disease 52 1.755
56
P CRV031 Cervical Adenocarcinoma 49 1.755
57
KRT008 Keratopathy 47 1.755
58
P MYG005 Myoglobinuria 44 1.755
59
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 1.241
60
MYL069 Myeloma, Multiple 85 1.241
61
c LKM061 Leukemia, Acute Myeloid 84 1.241
62
SQM013 Squamous Cell Carcinoma, Head and Neck 80 1.241
63
P LKM071 Leukemia, Chronic Lymphocytic 79 1.241
64
PLM134 Pulmonary Fibrosis, Idiopathic 77 1.241
65
LYM143 Lymphoma, Non-Hodgkin, Familial 72 1.241
66
P MTC003 Metachromatic Leukodystrophy 70 1.241
67
ODN023 Odontochondrodysplasia 68 1.241
68
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 68 1.241
69
P CNG001 Congenital Myasthenic Syndrome 66 1.241
70
LBR036 Leber Plus Disease 66 1.241
71
P LYS001 Loeys-Dietz Syndrome 65 1.241
72
c WLM013 Wilms Tumor 1 65 1.241
73
P CHR071 Charcot-Marie-Tooth Disease 65 1.241
74
NRM005 Neuromuscular Disease 64 1.241
75
P PLZ001 Pelizaeus-Merzbacher Disease 64 1.241
76
c ATS013 Autosomal Recessive Congenital Ichthyosis 63 1.241
77
P DST002 Distal Arthrogryposis 63 1.241
78
BLD131 Bladder Urothelial Carcinoma 62 1.241
79
P HRD011 Hereditary Spherocytosis 60 1.241
80
SPP011 Suppression of Tumorigenicity 12 59 1.241
81
EYD002 Eye Disease 58 1.241
82
P PRP019 Peripheral Nervous System Disease 58 1.241
83
P PRV006 Pervasive Developmental Disorder 57 1.241
84
c LKM070 Leukemia, Acute Monocytic 57 1.241
85
OVR012 Ovarian Serous Cystadenocarcinoma 56 1.241
86
KFM001 Kaufman Oculocerebrofacial Syndrome 56 1.241
87
FND002 Fundus Dystrophy 55 1.241
88
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 1.241
89
TXC002 Toxic Encephalopathy 53 1.241
90
OVR059 Ovary Adenocarcinoma 53 1.241
91
KGM001 Kagami-Ogata Syndrome 51 1.241
92
PLM135 Palmoplantar Keratoderma, Bothnian Type 51 1.241
93
c LYS018 Loeys-Dietz Syndrome 2 51 1.241
94
CRV040 Cervix Carcinoma 51 1.241
95
c HRD202 Hereditary Lymphedema I 50 1.241
96
P KLN006 Koolen-De Vries Syndrome 49 1.241
97
CMB003 Combined T Cell and B Cell Immunodeficiency 49 1.241
98
WLS003 Wilson-Turner X-Linked Mental Retardation Syndrome 49 1.241
99
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 48 1.241
100
DRG013 Drug-Induced Lupus Erythematosus 48 1.241
101
RCT020 Rectum Adenocarcinoma 48 1.241
102
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 47 1.241
103
ACT055 Actinomycosis 47 1.241
104
c CTR103 Cataract 4, Multiple Types 45 1.241
105
HNT019 Hantavirus Hemorrhagic Fever with Renal Syndrome 44 1.241
106
SPN369 Spinal Disease 43 1.241
107
P HRD018 Hair Disease 43 1.241
108
TNG004 Tongue Disease 42 1.241
109
CRB033 Cerebral Degeneration 42 1.241
110
c RTN041 Retinitis Pigmentosa 11 42 1.241
111
c HYP507 Hypotrichosis 1 39 1.241
112
P PRP021 Peripheral Nervous System Neoplasm 39 1.241
113
OVR047 Ovarian Cystadenocarcinoma 38 1.241
114
MSC190 Muscular Disease 37 1.241
115
c RTN052 Retinitis Pigmentosa 23 36 1.241
116
P LNS003 Lens Disease 34 1.241
117
OVR060 Ovary Epithelial Cancer 34 1.241
118
P HYP700 Hypomyelinating Leukodystrophy 33 1.241
119
PLN003 Plantar Fascial Fibromatosis 33 1.241
120
SPC003 Specific Developmental Disorder 31 1.241
121
c CTR097 Cataract 34, Multiple Types 31 1.241
122
INT379 Integumentary System Disease 28 1.241
123
c RTN053 Retinitis Pigmentosa 24 27 1.241
124
XLN228 X-Linked Recessive Disease 26 1.241
125
MLG076 Malignant Ovarian Surface Epithelial-Stromal Neoplasm 25 1.241
126
P ATN003 Autonomic Nervous System Neoplasm 25 1.241
127
c ATS009 Autosomal Genetic Disease 25 1.241
128
PLY179 Polyomavirus-Associated Nephropathy 24 1.241
129
EYD001 Eye Degenerative Disease 24 1.241
130
c XLN230 X-Linked Monogenic Disease 18 1.241
131
P GLM040 Glioma Susceptibility 1 81 0.082
132
GLB015 Glioblastoma Multiforme 75 0.082
133
P GLM045 Glioma 63 0.082
134
HYP066 Hyperglycemia 61 0.082
135
GLL048 Glial Tumor 45 0.082
136
c THY071 Thyroid Dyshormonogenesis 1 31 0.082
137
P LYM118 Lymphoma 68 0.067
138
P MCR115 Microvascular Complications of Diabetes 5 66 0.067
139
CHG001 Chagas Disease 66 0.067
140
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.067
141
c HPT003 Hepatitis a 62 0.067
142
ATM095 Autoimmune Disease 62 0.067
143
P DNG005 Dengue Virus 59 0.067
144
ONC002 Onchocerciasis 52 0.067
145
TRM010 Traumatic Brain Injury 51 0.067
146
STM007 Stomatitis 50 0.067
147
VLV047 Volvulus of Midgut 49 0.067
148
CRB004 Cerebral Artery Occlusion 45 0.067
149
48X005 48,xyyy 39 0.067
150
c THY056 Thyroid Dyshormonogenesis 3 30 0.067
151
ESP021 Esophageal Cancer 90 0.047
152
c SYS001 Systemic Lupus Erythematosus 86 0.047
153
P GST053 Gastric Cancer 83 0.047
154
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.047
155
ULC004 Ulcerative Colitis 73 0.047
156
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.047
157
c HPT073 Hepatitis C Virus 72 0.047
158
P LVR013 Liver Disease 68 0.047
159
P PLM037 Pulmonary Hypertension 67 0.047
160
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.047
161
LNG039 Lung Squamous Cell Carcinoma 66 0.047
162
PRT036 Peritonitis 64 0.047
163
P PRD008 Periodontitis 64 0.047
164
P ADN016 Adenocarcinoma 64 0.047
165
LSH001 Leishmaniasis 63 0.047
166
c ALP101 Alpha-Thalassemia 62 0.047
167
c SVR001 Severe Acute Respiratory Syndrome 62 0.047
168
MDD011 Mood Disorder 62 0.047
169
TXC005 Toxic Shock Syndrome 62 0.047
170
P ENC004 Encephalitis 61 0.047
171
P PNC044 Pancreatitis 61 0.047
172
VRL011 Viral Infectious Disease 61 0.047
173
P LPS004 Lupus Erythematosus 61 0.047
174
P KDN017 Kidney Cancer 60 0.047
175
P SCL018 Scoliosis 60 0.047
176
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.047
177
c ACT027 Acute Pancreatitis 60 0.047
178
LNG099 Lung Disease 60 0.047
179
P CTR002 Cataract 60 0.047
180
P THL005 Thalassemia 60 0.047
181
P SYP003 Syphilis 58 0.047
182
ISC004 Ischemia 58 0.047
183
P BCL017 B-Cell Lymphoma 58 0.047
184
P INF032 Infertility 57 0.047
185
P GLM007 Glomerulonephritis 57 0.047
186
VSC002 Vascular Dementia 57 0.047
187
JPN002 Japanese Encephalitis 57 0.047
188
HYP266 Hypoxia 57 0.047
189
P CHN012 Chondrosarcoma 56 0.047
190
LST001 Listeriosis 56 0.047
191
BCT022 Bacterial Infectious Disease 56 0.047
192
P SZR006 Seizure Disorder 56 0.047
193
AGN016 Aging 56 0.047
194
VSC003 Visceral Leishmaniasis 55 0.047
195
DFF005 Diffuse Large B-Cell Lymphoma 55 0.047
196
FLR002 Filariasis 55 0.047
197
HYP060 Hyperinsulinism 54 0.047
198
P LTR001 Lateral Sclerosis 54 0.047
199
HMS001 Hemosiderosis 54 0.047
200
P RNL017 Renal Oncocytoma 53 0.047
201
c PRD040 Periodontitis, Chronic 53 0.047
202
CLR109 Colorectal Adenocarcinoma 51 0.047
203
CCC002 Coccidiosis 51 0.047
204
P AST007 Astrocytoma 51 0.047
205
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.047
206
AZS001 Azoospermia 50 0.047
207
ONC007 Oncocytoma 49 0.047
208
CCN002 Cocaine Abuse 49 0.047
209
BRN071 Brain Injury 49 0.047
210
c HPT015 Hepatitis D 49 0.047
211
VCC001 Vaccinia 49 0.047
212
BNR002 Bone Resorption Disease 48 0.047
213
HLX001 Helix Syndrome 47 0.047
214
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.047
215
CYT002 Cytokine Deficiency 42 0.047
216
IDP070 Idiopathic Scoliosis 42 0.047
217
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.047
218
P KLZ004 Kala-Azar 1 41 0.047
219
P RRH023 Rare Hereditary Hemochromatosis 41 0.047
220
P SPR119 Spermatogenic Failure, X-Linked, 1 39 0.047
221
c ACT079 Acute Proliferative Glomerulonephritis 39 0.047
222
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.047
223
LWG005 Low-Grade Astrocytoma 38 0.047
224
c RTN129 Retinitis Pigmentosa 49 37 0.047
225
ACT040 Acute Poststreptococcal Glomerulonephritis 36 0.047
226
WRT003 Warthin Tumor 34 0.047
227
PRX085 Preaxial Hallucal Polydactyly 28 0.047
228
TBL029 Tubulin, Beta 28 0.047
229
MMM002 Mammary-Digital-Nail Syndrome 23 0.047
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