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Search results for NADP

586 hits were found for NADP

# Family MCID Name MIFTS Score
1
24D001 2,4-Dienoyl-Coa Reductase Deficiency 35 2.760
2
HLX001 Helix Syndrome 47 2.555
3
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 2.490
4
P HML002 Hemolytic Anemia 62 2.159
5
GLM045 Glioma 62 1.873
6
GLL048 Glial Tumor 51 1.640
7
FTT001 Fatty Liver Disease 61 1.482
8
PPL052 Papillomatosis, Confluent and Reticulated 34 1.438
9
P PLL002 Pellagra 46 1.391
10
HYP066 Hyperglycemia 60 1.378
11
LPT001 Leptospirosis 65 1.368
12
P TXP001 Toxoplasmosis 59 1.368
13
P MYC084 Mycobacterium Tuberculosis 1 68 1.352
14
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 1.351
15
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.339
16
PRT037 Pertussis 49 1.339
17
CHL014 Cholera 62 1.310
18
PST092 Posttransplant Acute Limbic Encephalitis 29 1.310
19
P GLM040 Glioma Susceptibility 1 70 1.295
20
HYP266 Hypoxia 56 1.289
21
MLG169 Malignant Astrocytoma 57 1.279
22
MLR004 Malaria 77 1.228
23
HYP056 Hypoglycemia 65 1.228
24
ANX004 Anoxia 40 1.219
25
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 1.209
26
GLB002 Glioblastoma 67 1.187
27
CND006 Candida Glabrata 29 1.167
28
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.129
29
P MYC008 Myocarditis 59 1.117
30
P HRD144 Hereditary Mixed Polyposis Syndrome 54 1.103
31
P NRB001 Neuroblastoma 66 1.062
32
HMP009 Haemophilus Influenzae 41 1.062
33
IRN002 Iron Metabolism Disease 56 1.033
34
NNT012 Neonatal Jaundice 53 1.001
35
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.966
36
INS001 Insulinoma 59 0.966
37
ATH013 Atherosclerosis Susceptibility 63 0.947
38
GRD001 Giardiasis 46 0.947
39
CRT066 Cortisone Reductase Deficiency 2 23 0.941
40
ISC004 Ischemia 61 0.926
41
ANT024 Anthrax Disease 57 0.926
42
P CTN015 Cutaneous T Cell Lymphoma 48 0.905
43
P TRM004 Trimethylaminuria 45 0.905
44
QFV001 Q Fever 61 0.905
45
HYP005 Hypokalemia 55 0.905
46
PST011 Pustulosis of Palm and Sole 52 0.905
47
P PSR002 Psoriasis 63 0.905
48
47X002 47,xyy 47 0.905
49
CMB083 Combined Immunodeficiency and Megaloblastic Anemia with or Without Hyperhomocysteinemia 28 0.881
50
OCL069 Ocular Motor Apraxia 57 0.881
51
VLV047 Volvulus of Midgut 55 0.881
52
TXC005 Toxic Shock Syndrome 61 0.881
53
P LCT001 Lactic Acidosis 50 0.881
54
DBT010 Diabetic Neuropathy 54 0.881
55
P MSC005 Muscular Dystrophy 66 0.881
56
P HYP769 Hyperlysinemia, Type I 42 0.855
57
NRR001 Neuroretinitis 42 0.855
58
P MLN008 Melanoma 75 0.855
59
RTN023 Retinitis 45 0.855
60
c RNG015 Ring Chromosome 2 22 0.855
61
c MCR133 Microvascular Complications of Diabetes 4 41 0.825
62
c MCR113 Microvascular Complications of Diabetes 3 52 0.825
63
c MCR130 Microvascular Complications of Diabetes 6 41 0.825
64
c MCR120 Microvascular Complications of Diabetes 7 47 0.825
65
HMS001 Hemosiderosis 48 0.825
66
HYP026 Hypoglycemic Coma 37 0.825
67
HGH043 High Grade Glioma 46 0.825
68
RCK004 Rickets 64 0.825
69
CMP034 Complete Androgen Insensitivity Syndrome 55 0.825
70
P URT039 Urticaria 57 0.825
71
PYR009 Pyridoxine Deficiency Anemia 35 0.825
72
MSC157 Muscular Dystrophy, Duchenne Type 78 0.790
73
c CHR708 Chronic Urticaria 42 0.790
74
ANP005 Anaplastic Astrocytoma 59 0.790
75
DRM006 Dermatitis 61 0.790
76
P RTN016 Retinal Degeneration 52 0.790
77
P RRH023 Rare Hereditary Hemochromatosis 52 0.790
78
P HYP265 Hypotonia 42 0.790
79
P CRC039 Coarctation of Aorta 46 0.744
80
CLN015 Colon Adenocarcinoma 64 0.744
81
VCC001 Vaccinia 49 0.744
82
CCC002 Coccidiosis 50 0.744
83
ADN018 Adenoma 58 0.744
84
PLM001 Pulmonary Tuberculosis 69 0.744
85
DVR002 Diverticulitis 46 0.744
86
MYX004 Myxedema 43 0.633
87
c BSL007 Basal Cell Carcinoma 67 0.633
88
CRN036 Craniopharyngioma 63 0.633
89
SNL007 Senile Cataract 40 0.633
90
c LKM061 Leukemia, Acute Myeloid 83 0.520
91
48X005 48,xyyy 39 0.508
92
CNG017 Congenital Nonspherocytic Hemolytic Anemia 34 0.470
93
P CHR012 Chronic Granulomatous Disease 69 0.470
94
APP015 Apparent Mineralocorticoid Excess 57 0.443
95
DFC004 Deficiency Anemia 74 0.414
96
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.414
97
SLP001 Sleeping Sickness 56 0.399
98
P HYP086 Hypothyroidism 68 0.384
100
P BLD134 Bladder Cancer 79 0.350
101
P LNG064 Lung Cancer Susceptibility 3 69 0.350
102
LPD008 Lipid Metabolism Disorder 61 0.350
103
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.332
104
END057 Endometrial Cancer 76 0.332
105
DPH001 Diphtheria 59 0.332
106
HYP060 Hyperinsulinism 53 0.332
107
P MYL006 Myeloid Leukemia 60 0.332
108
MTB004 Metabolic Acidosis 48 0.313
109
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.313
110
BLR008 Bilirubin Metabolic Disorder 57 0.313
111
CHG001 Chagas Disease 65 0.313
112
P BCL017 B-Cell Lymphoma 57 0.313
113
P SCK005 Sickle Cell Disease 56 0.313
114
P HYP076 Hyperthyroidism 53 0.313
115
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.313
116
P OVR042 Ovarian Cancer 88 0.293
117
OST159 Osteogenic Sarcoma 66 0.293
118
AGN016 Aging 53 0.293
119
P PNC035 Pancreatic Cancer 87 0.293
120
LKC009 Leukocyte Adhesion Deficiency, Type I 69 0.293
121
TRY001 Trypanosomiasis 50 0.293
122
P LKM002 Leukemia 65 0.293
123
PNC129 Pancreatic Adenocarcinoma 64 0.293
124
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.293
125
BRN071 Brain Injury 50 0.293
126
THY029 Thyroid Carcinoma 55 0.293
127
P GST053 Gastric Cancer 82 0.271
128
P ATX030 Ataxia-Telangiectasia 80 0.271
129
CHL065 Cholangiocarcinoma 57 0.271
130
P HPT023 Hepatocellular Carcinoma 95 0.271
131
DFF005 Diffuse Large B-Cell Lymphoma 55 0.271
132
P OLG002 Oligodendroglioma 66 0.271
133
P MYP004 Myopathy 67 0.271
134
P PLM036 Pulmonary Fibrosis 65 0.271
135
INT079 Intrahepatic Cholangiocarcinoma 51 0.271
136
TLN003 Telangiectasis 51 0.271
137
P OVR046 Ovarian Cyst 43 0.271
138
DWR001 Dwarfism 44 0.271
139
P ENC018 Encephalopathy 62 0.271
140
CLT003 Colitis 63 0.248
141
NRL016 Neural Tube Defects 80 0.248
142
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.248
143
c ATR087 Atrial Standstill 1 74 0.248
144
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.248
145
TRC008 Trachoma 53 0.248
146
NNL006 Non-Alcoholic Steatohepatitis 54 0.248
147
P BNG032 Benign Mesothelioma 53 0.248
148
P FBR017 Fibrosarcoma 55 0.248
149
P BRB001 Beriberi 44 0.248
150
BCT022 Bacterial Infectious Disease 55 0.248
151
P HRT032 Heart Disease 84 0.248
152
P GLM007 Glomerulonephritis 59 0.248
153
P LVR013 Liver Disease 68 0.248
154
BLD131 Bladder Urothelial Carcinoma 59 0.248
155
P BRS044 Breast Adenocarcinoma 58 0.248
156
PRS045 Prostatic Hypertrophy 53 0.248
157
CHR074 Choriocarcinoma 46 0.248
158
PRT036 Peritonitis 65 0.248
159
TRM010 Traumatic Brain Injury 50 0.248
160
ORG002 Organic Acidemia 43 0.222
161
BRN032 Brain Glioma 45 0.222
162
c TYP009 Type 2 Diabetes Mellitus 91 0.222
163
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.222
164
P CLR023 Colorectal Cancer 100 0.222
165
SPP011 Suppression of Tumorigenicity 12 61 0.222
166
c HYP602 Hyperoxaluria, Primary, Type Ii 51 0.222
167
P RTN008 Retinitis Pigmentosa 79 0.222
168
c HYP836 Hypercholesterolemia, Familial, 1 73 0.222
169
ESP021 Esophageal Cancer 84 0.222
170
HRW001 Hair Whorl 35 0.222
171
PRS129 Prostatic Hyperplasia, Benign 48 0.222
172
BTN004 Biotin Deficiency 44 0.222
173
UTR056 Uterine Corpus Endometrial Carcinoma 28 0.222
174
END075 Endocervical Adenocarcinoma 37 0.222
175
P PRM002 Primary Hyperoxaluria 65 0.222
176
P PYL005 Pyelonephritis 56 0.222
177
CRV038 Cervical Squamous Cell Carcinoma 56 0.222
178
P ADN016 Adenocarcinoma 63 0.222
179
PRS021 Prostatic Adenoma 43 0.222
180
LNG039 Lung Squamous Cell Carcinoma 57 0.222
181
NRD001 Neurodermatitis 39 0.222
182
GTR002 Goiter 52 0.222
183
c PRC016 Pre-Eclampsia 64 0.222
184
PLS007 Plasmodium Falciparum Malaria 52 0.222
185
DYS015 Dysentery 49 0.222
186
P CTR002 Cataract 59 0.222
187
ALL006 Allergic Asthma 55 0.222
188
SKN019 Skin Melanoma 70 0.222
189
DGN001 Degenerative Disc Disease 48 0.222
190
CHL045 Choline Deficiency Disease 39 0.222
191
P CRN300 Coronary Heart Disease 1 73 0.192
192
MYL009 Myelodysplastic Syndrome 67 0.192
193
P RHM011 Rheumatoid Arthritis 81 0.192
194
P SRC025 Sarcoidosis 1 70 0.192
195
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.192
196
P GLC113 Galactosemia I 65 0.192
197
PYR041 Pyruvate Kinase Deficiency of Red Cells 56 0.192
198
P BRS047 Breast Cancer 97 0.192
199
c 2HY001 2-Hydroxyglutaric Aciduria 38 0.192
200
P PLM037 Pulmonary Hypertension 69 0.192
201
MSC007 Muscle Hypertrophy 64 0.192
202
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.192
203
P SPP010 Suppressor of Tumorigenicity 3 50 0.192
204
URT049 Urate Oxidase, Pseudogene 24 0.192
205
P LNG032 Lung Cancer 98 0.192
206
DGL002 D-Glyceric Aciduria 40 0.192
207
MYL005 Myelofibrosis 70 0.192
208
c MCR115 Microvascular Complications of Diabetes 5 65 0.192
209
c PCH010 Pachyonychia Congenita 3 43 0.192
210
MLD001 Melioidosis 67 0.192
211
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.192
212
c HYP595 Hypertension, Essential 84 0.192
213
FRC001 Fructose-1,6-Bisphosphatase Deficiency 50 0.192
214
c RTN130 Retinitis Pigmentosa 46 40 0.192
215
ORN001 Ornithosis 39 0.192
216
FDL002 Food Allergy 47 0.192
217
SQM006 Squamous Cell Carcinoma 59 0.192
218
CHL068 Cholestasis 61 0.192
219
DBT007 Diabetic Cataract 36 0.192
220
P ECL001 Eclampsia 52 0.192
221
P PRP019 Peripheral Nervous System Disease 57 0.192
222
P LTR001 Lateral Sclerosis 57 0.192
223
FML063 Familial Glucocorticoid Deficiency 58 0.192
224
P EPL164 Epilepsy 70 0.192
225
P SKN015 Skin Carcinoma 71 0.192
226
P PNC044 Pancreatitis 61 0.192
227
c ACT027 Acute Pancreatitis 60 0.192
228
GLC003 Glucose Intolerance 53 0.192
229
TXC004 Toxic Diffuse Goiter 24 0.192
230
ACT003 Acute Kidney Tubular Necrosis 46 0.192
231
P CRD246 Cardiovascular System Disease 55 0.192
232
CRB004 Cerebral Artery Occlusion 45 0.192
233
P ART022 Arthritis 70 0.192
234
c CNG027 Congenital Hemolytic Anemia 49 0.192
235
GST040 Gastric Adenocarcinoma 66 0.192
236
BRN056 Bronchopulmonary Dysplasia 57 0.192
237
P DBT009 Diabetes Mellitus 67 0.192
238
ULC004 Ulcerative Colitis 74 0.192
239
P PRD008 Periodontitis 63 0.192
240
P NRP001 Neuropathy 59 0.192
241
CRL001 Cerulean Cataract 26 0.192
242
CLP006 Clopidogrel Resistance 44 0.192
243
RFR010 Refractory Anemia 49 0.192
244
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.157
245
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.157
246
P CRD119 Cardiac Arrest 68 0.157
247
P LYM118 Lymphoma 66 0.157
248
P ALZ034 Alzheimer Disease 87 0.157
249
DWN001 Down Syndrome 70 0.157
250
P MDL005 Medulloblastoma 75 0.157
251
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.157
252
P RTN024 Retinoblastoma 72 0.157
253
c L2H001 L-2-Hydroxyglutaric Aciduria 49 0.157
254
FND001 Fundus Albipunctatus 56 0.157
255
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.157
256
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.157
257
c BRN108 Branchiootic Syndrome 1 63 0.157
259
P MCR129 Microvascular Complications of Diabetes 1 67 0.157
260
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.157
261
DSS032 Disease by Infectious Agent 55 0.157
262
P SML001 Small Cell Carcinoma 52 0.157
263
c MCR112 Microvascular Complications of Diabetes 2 42 0.157
264
P CHN012 Chondrosarcoma 56 0.157
265
c GLL024 Gallbladder Disease 1 53 0.157
266
P MYC007 Myocardial Infarction 69 0.157
267
MNN043 Meningioma, Familial 79 0.157
268
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 44 0.157
269
RBF001 Riboflavin Deficiency 49 0.157
270
P PRK057 Parkinson Disease, Late-Onset 79 0.157
271
P HNT016 Huntington Disease 73 0.157
272
P FRD001 Friedreich Ataxia 62 0.157
273
FRC013 Fructose Utilization 15 0.157
274
ASP030 Aspirin Resistance 41 0.157
275
P KLZ004 Kala-Azar 1 41 0.157
276
BNR002 Bone Resorption Disease 47 0.157
277
CHL123 Chlamydia 58 0.157
278
LWG006 Low Grade Glioma 41 0.157
279
P PLY014 Polycystic Kidney Disease 71 0.157
280
CLR109 Colorectal Adenocarcinoma 50 0.157
281
P ART021 Arteriosclerosis 53 0.157
282
TLR001 Tularemia 56 0.157
283
BRS099 Breast Ductal Carcinoma 61 0.157
284
KRT009 Keratosis 52 0.157
285
P ICH004 Ichthyosis 56 0.157
286
ANG046 Angioimmunoblastic T-Cell Lymphoma 50 0.157
287
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.157
288
CLR030 Clear Cell Renal Cell Carcinoma 53 0.157
289
P ACN011 Acne 55 0.157
290
RYS001 Reye Syndrome 49 0.157
291
IRN001 Iron Deficiency Anemia 58 0.157
292
P OPT006 Optic Nerve Disease 57 0.157
293
P PLY019 Polyneuropathy 52 0.157
294
P BNG002 Benign Meningioma 36 0.157
295
SCR001 Secretory Meningioma 40 0.157
296
CRC021 Carcinosarcoma 62 0.157
297
P GST044 Gastritis 55 0.157
298
GST010 Gestational Trophoblastic Neoplasm 52 0.157
299
ART016 Aortic Aneurysm 68 0.157
300
ALC006 Alcoholic Hepatitis 61 0.157
301
DBT002 Diabetic Autonomic Neuropathy 40 0.157
302
P OPN001 Open-Angle Glaucoma 55 0.157
303
c ACT073 Acute Leukemia 59 0.157
304
URL001 Urolithiasis 45 0.157
305
INT395 Intracranial Meningioma 47 0.157
306
HST011 Histoplasmosis 54 0.157
307
OLV001 Olivopontocerebellar Atrophy 50 0.157
308
GT001 Gout 63 0.157
309
P PRN023 Prion Disease 60 0.157
310
c INH020 Inherited Metabolic Disorder 47 0.157
311
SKN016 Skin Disease 63 0.157
312
CHL061 Childhood Leukemia 47 0.157
313
RSC001 Rosacea 55 0.157
314
LSH001 Leishmaniasis 63 0.157
315
P LCH002 Lichen Planus 54 0.157
316
INT040 Intrinsic Asthma 36 0.157
317
STM007 Stomatitis 52 0.157
318
CRH001 Crohn's Disease 80 0.157
320
ALL014 Allergic Encephalomyelitis 34 0.157
321
ANR040 Aneurysm 60 0.157
322
STN013 Stenotrophomonas Maltophilia Infection 26 0.157
323
P HRP006 Herpes Simplex 65 0.157
324
HGH041 High-Grade Astrocytoma 36 0.157
325
PLY100 Polyploidy 36 0.157
326
P SMP003 Simpson-Golabi-Behmel Syndrome 49 0.157
327
ARG004 Argyria 26 0.157
328
RFR009 Refractory Cytopenia with Multilineage Dysplasia 30 0.157
329
ACT168 Acute Annular Outer Retinopathy 10 0.157
330
CNG393 Congenital Muscular Dystrophy with Hyperlaxity 12 0.157
331
PRM329 Premature Aging 36 0.157
332
MYL020 Myelomeningocele 51 0.111
333
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.111
334
HMM004 Hamamy Syndrome 39 0.111
335
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 0.111
336
c NMN014 Niemann-Pick Disease, Type C2 49 0.111
337
CRH005 Crohn's Colitis 53 0.111
338
P APL001 Aplastic Anemia 72 0.111
339
RNL077 Renal Fibrosis 46 0.111
340
PRP001 Propionic Acidemia 65 0.111
341
HYP003 Hypermethioninemia 51 0.111
342
P INF037 Inflammatory Bowel Disease 53 0.111
343
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.111
344
P SCH015 Schizophrenia 74 0.111
345
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 0.111
346
CYS001 Cystic Fibrosis 77 0.111
347
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.111
348
c MGR028 Migraine with or Without Aura 1 63 0.111
349
OTT002 Otitis Media 70 0.111
350
c GLC079 Glaucoma 1, Open Angle, P 23 0.111
351
P HYP605 Hyperphenylalaninemia, Bh4-Deficient, B 44 0.111
352
HYD030 Hydroxykynureninuria 27 0.111
353
P MPL001 Maple Syrup Urine Disease 69 0.111
354
MTH074 Methionine Adenosyltransferase I/iii Deficiency 43 0.111
355
ALC007 Alcohol Dependence 65 0.111
356
c HYP731 Hyperaldosteronism, Familial, Type I 59 0.111
357
c PRD040 Periodontitis, Chronic 52 0.111
358
LSC001 Lesch-Nyhan Syndrome 62 0.111
359
ICH054 Ichthyosis, X-Linked 51 0.111
360
c PRK090 Parkinson Disease 3, Autosomal Dominant 38 0.111
361
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.111
362
c MCR245 Microphthalmia, Syndromic 8 46 0.111
363
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.111
364
HMC014 Homocysteinemia 52 0.111
365
PHS014 Phosphoglycerate Kinase 1 Deficiency 46 0.111
366
P D2H002 D-2-Hydroxyglutaric Aciduria 1 53 0.111
367
P NSP012 Nasopharyngeal Carcinoma 60 0.111
368
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.111
369
ANX010 Anxiety 70 0.111
370
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 0.111
371
P FML011 Familial Adenomatous Polyposis 70 0.111
372
HYP025 Hyperphosphatemia 47 0.111
373
c PRM032 Primary Congenital Glaucoma 40 0.111
374
FML037 Female Breast Cancer 51 0.111
375
ATS010 Autosomal Recessive Disease 42 0.111
376
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.111
377
c DFN134 Deafness, Autosomal Dominant 40 22 0.111
378
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.111
379
KSH004 Kashin-Beck Disease 37 0.111
380
c FST017 Fasting Plasma Glucose Level Quantitative Trait Locus 5 12 0.111
381
CYN002 Cyanosis, Transient Neonatal 43 0.111
382
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.111
383
c DFN360 Deafness, Autosomal Dominant 69 34 0.111
384
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.111
385
P EXN002 Exanthem 58 0.111
386
HYP001 Hypochromic Microcytic Anemia 36 0.111
389
c THY107 Thymoma, Familial 42 0.111
390
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.111
391
ANN002 Anencephaly 57 0.111
392
BLD065 Blue Diaper Syndrome 20 0.111
393
P HYP750 Hypertriglyceridemia, Familial 61 0.111
394
PCK003 Pick Disease of Brain 70 0.111
395
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 0.111
396
GRG001 Greig Cephalopolysyndactyly Syndrome 64 0.111
397
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.111
398
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 56 0.111
399
HMC042 Homocystinuria-Megaloblastic Anemia, Cble Complementation Type 34 0.111
400
IMM167 Immune Deficiency Disease 76 0.111
401
HRT031 Hartnup Disorder 51 0.111
402
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.111
403
P LPR021 Leprosy 3 71 0.111
404
MTH071 Methane Production 24 0.111
405
PHN003 Phenylketonuria 76 0.111
406
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 57 0.111
407
TRC120 Tricarboxylic Acid Cycle, Defect of 15 0.111
408
MST021 Meester-Loeys Syndrome 37 0.111
409
P WSK001 Wiskott-Aldrich Syndrome 72 0.111
410
P AST005 Asthma 75 0.111
411
P LKM062 Leukemia, Acute Lymphoblastic 69 0.111
412
P PRK101 Parkinsonism-Dystonia, Infantile, 1 40 0.111
413
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.111
415
c NPH068 Nephronophthisis 16 44 0.111
416
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.111
417
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.111
418
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 42 0.111
419
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 50 0.111
420
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 52 0.111
421
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.111
422
c D2H003 D-2-Hydroxyglutaric Aciduria 2 36 0.111
423
c BTT014 Beta-Thalassemia 72 0.111
424
ATM095 Autoimmune Disease 61 0.111
425
P LKM071 Leukemia, Chronic Lymphocytic 74 0.111
426
CLF027 Cleft Palate, Isolated 64 0.111
427
CRT072 Creutzfeldt-Jakob Disease 67 0.111
428
GLB001 Gilbert Syndrome 53 0.111
429
c MST023 Mesothelioma, Malignant 56 0.111
430
c TBL031 Tubulointerstitial Kidney Disease, Autosomal Dominant, 1 48 0.111
431
P PHC003 Pheochromocytoma 70 0.111
432
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.111
433
c BRT028 Brittle Cornea Syndrome 1 39 0.111
434
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.111
435
CRV035 Cervical Cancer 72 0.111
436
c SPS094 Spastic Paraplegia 29, Autosomal Dominant 29 0.111
437
ONC007 Oncocytoma 49 0.111
438
HLC007 Helicobacter Pylori Infection 67 0.111
439
P FTL001 Fetal Alcohol Syndrome 55 0.111
440
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 0.111
441
KSH001 Keshan Disease 31 0.111
442
ADR040 Adrenal Gland Pheochromocytoma 45 0.111
443
STN011 Sting-Associated Vasculopathy with Onset in Infancy 44 0.111
444
LBR036 Leber Plus Disease 67 0.111
445
P SNS001 Sensorineural Hearing Loss 60 0.111
446
THY128 Thyroid Tumor 33 0.111
447
CTS002 Cat-Scratch Disease 42 0.111
448
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.111
449
ONC002 Onchocerciasis 50 0.111
450
P HYP111 Hyperprolinemia 44 0.111
451
CLR108 Colorectal Adenoma 63 0.111
452
THY006 Thymus Lymphoma 27 0.111
453
P CYS018 Cystitis 58 0.111
454
P DDN001 Duodenal Ulcer 52 0.111
455
DRG002 Drug-Induced Hepatitis 42 0.111
456
P GCH001 Gaucher's Disease 69 0.111
457
ACT078 Acute Porphyria 50 0.111
458
P TMP001 Temporal Lobe Epilepsy 49 0.111
459
P THY023 Thymoma 64 0.111
460
SCK001 Sick Building Syndrome 33 0.111
461
P CYS039 Cystic Kidney Disease 52 0.111
462
PRS036 Parasitic Protozoa Infectious Disease 44 0.111
463
PLM029 Palmoplantar Keratosis 48 0.111
464
P KRN004 Kernicterus 47 0.111
465
P VSC007 Vascular Disease 62 0.111
466
HYP014 Hyperuricemia 51 0.111
467
TRC003 Trichomoniasis 53 0.111
468
LYM021 Lymphadenitis 55 0.111
469
CRT020 Cortisone Reductase Deficiency 36 0.111
470
MSN003 Mesenteric Vascular Occlusion 24 0.111
471
URT010 Ureteral Obstruction 44 0.111
472
P PLC011 Pilocytic Astrocytoma 55 0.111
473
MST004 Mast Cell Neoplasm 41 0.111
474
INT020 Intravenous Leiomyomatosis 35 0.111
475
LMY003 Leiomyomatosis 43 0.111
476
CNG034 Congestive Heart Failure 69 0.111
477
RCT015 Reactive Arthritis 60 0.111
478
P CND004 Candidiasis 57 0.111
479
ACT098 Acute Erythroid Leukemia 55 0.111
480
P URN019 Urinary Tract Infection 48 0.111
481
c VRL010 Viral Hepatitis 52 0.111
482
c FML021 Familial Hypercholesterolemia 71 0.111
483
P OVR049 Ovarian Disease 50 0.111
484
LCH001 Leech Infestation 37 0.111
485
P PRP029 Porphyria 60 0.111
486
MGL001 Megaloblastic Anemia 59 0.111
487
TYP007 Typhoid Fever 63 0.111
488
PRS042 Prostate Disease 42 0.111
489
P SYS005 Systemic Scleroderma 73 0.111
490
EBL001 Ebola Hemorrhagic Fever 55 0.111
491
NRM005 Neuromuscular Disease 62 0.111
492
ADR005 Adrenal Carcinoma 58 0.111
493
SNS003 Sensory Peripheral Neuropathy 51 0.111
494
TRT001 Teratocarcinoma 41 0.111
495
PSD007 Pseudomyxoma Peritonei 52 0.111
496
PLM014 Pleomorphic Adenoma 51 0.111
497
MCP006 Mucoepidermoid Carcinoma 48 0.111
498
EXT007 Extracutaneous Mastocytoma 38 0.111
499
TST014 Testicular Cancer 51 0.111
500
P HYP061 Hypertrophic Cardiomyopathy 68 0.111
501
ALL029 Allergic Disease 61 0.111
502
PRM236 Primary Biliary Cholangitis 62 0.111
503
P ADL010 Adult Respiratory Distress Syndrome 70 0.111
504
LST001 Listeriosis 59 0.111
505
NPH010 Nephrosclerosis 50 0.111
506
GST033 Gestational Diabetes 60 0.111
507
CHR073 Choreatic Disease 53 0.111
508
c ACT068 Acute Cystitis 60 0.111
509
P RNL015 Renal Hypertension 45 0.111
510
FLR002 Filariasis 55 0.111
511
P HYD006 Hydrocephalus 62 0.111
512
P HYP024 Hypoparathyroidism 55 0.111
513
MCR018 Microcytic Anemia 46 0.111
514
P NPH005 Nephronophthisis 59 0.111
515
CVD001 Covid-19 59 0.111
516
LGN002 Legionellosis 61 0.111
517
P MTH008 Methylmalonic Acidemia 52 0.111
518
RHM001 Rheumatic Fever 59 0.111
519
SCH014 Schistosomiasis 56 0.111
520
P NMN002 Niemann-Pick Disease 60 0.111
521
P DMN002 Dementia 65 0.111
522
NNT010 Nontoxic Goiter 32 0.111
523
FLR001 Filarial Elephantiasis 59 0.111
524
PRN009 Paranoid Schizophrenia 49 0.111
525
VRC001 Varicocele 48 0.111
526
P INF032 Infertility 60 0.111
527
P SLP005 Sleep Disorder 61 0.111
528
SCR011 Scrapie 39 0.111
529
P RNL017 Renal Oncocytoma 54 0.111
530
LNG031 Lung Benign Neoplasm 51 0.111
531
BRN024 Bronchitis 67 0.111
532
ACQ007 Acquired Immunodeficiency Syndrome 58 0.111
533
c JVN010 Juvenile Rheumatoid Arthritis 52 0.111
534
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 0.111
535
PRM209 Primary Trimethylaminuria 19 0.111
536
P HMC002 Homocystinuria 52 0.111
537
VRL011 Viral Infectious Disease 60 0.111
538
P ATR005 Atrophic Gastritis 50 0.111
539
BBS001 Babesiosis 48 0.111
540
VSC003 Visceral Leishmaniasis 54 0.111
541
AMB001 Amebiasis 56 0.111
542
CLF001 Cleft Lip 54 0.111
543
P ZLL001 Zellweger Syndrome 65 0.111
544
P MLG056 Malignant Hyperthermia 65 0.111
545
PPT005 Peptic Ulcer Disease 58 0.111
546
P MSC003 Muscular Atrophy 52 0.111
547
P MNC007 Monocytic Leukemia 48 0.111
548
P INF038 Influenza 68 0.111
549
LNG099 Lung Disease 62 0.111
550
FND002 Fundus Dystrophy 54 0.111
551
CYT002 Cytokine Deficiency 43 0.111
552
GLC039 Glucosephosphate Isomerase Deficiency 17 0.111
553
HNS001 Hansen's Disease 32 0.111
554
CHC001 Chickenpox 56 0.111
555
P HYP098 Hypereosinophilic Syndrome 66 0.111
556
ALB002 Albinism 46 0.111
557
RFC001 Rfc1 Canvas / Spectrum Disorder 5 0.111
558
c NNS007 Nonsyndromic Deafness 36 0.111
559
CRT015 Carotid Artery Occlusion 45 0.111
560
c CNG216 Congenital Hydrocephalus 50 0.111
561
P THL005 Thalassemia 56 0.111
562
LPD009 Lipid Storage Disease 45 0.111
563
P OTT001 Otitis Externa 43 0.111
564
c BCT007 Bacterial Meningitis 55 0.111
565
P MNN013 Meningitis 65 0.111
566
c SPS035 Spastic Paraplegia 29 13 0.111
567
WLL004 Wallerian Degeneration 38 0.111
569
CRC006 Carcinoid Syndrome 55 0.111
570
OVR094 Ovarian Epithelial Cancer 39 0.111
571
PTT041 Pituitary Stalk Interruption Syndrome 54 0.111
572
CHR178 Chromosomal Triplication 33 0.111
573
FST010 Fasting Hypoglycemia 33 0.111
574
HVY002 Heavy Metal Poisoning 22 0.111
575
HYP835 Hypothalamic Obesity 38 0.111
576
DRG003 Drug Dependence 46 0.111
577
FCL090 Facial Cleft 32 0.111
578
c INH030 Inherited Retinal Disorder 28 0.111
579
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 38 0.111
580
HVY003 Heavy Chain Deposition Disease 18 0.111
581
ACT162 Acute Sensory Ataxic Neuropathy 24 0.111
582
PRQ002 Paraquat Poisoning 28 0.111
583
MTH046 Methylmalonic Acidemia Without Homocystinuria 39 0.111
584
P SPN237 Spina Bifida Aperta 19 0.111
585
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.111
586
c ACT134 Acute Liver Failure 57 0.111
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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