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Search results for Phosphoribosyl pyrophosphate

348 hits were found for Phosphoribosyl pyrophosphate

# Family MCID Name MIFTS Score
1
LSC001 Lesch-Nyhan Syndrome 62 21.663
2
GT001 Gout 64 18.422
3
IRN002 Iron Metabolism Disease 57 11.674
4
P KDN018 Kidney Disease 72 11.331
5
c CHR684 Chronic Kidney Disease 69 10.884
6
BNR002 Bone Resorption Disease 47 9.349
7
HYP014 Hyperuricemia 51 8.469
8
P AMY004 Amyloidosis 70 8.261
9
P ART022 Arthritis 71 8.132
10
END086 End Stage Renal Disease 52 7.720
11
ADN024 Adenine Phosphoribosyltransferase Deficiency 53 7.393
12
DFC004 Deficiency Anemia 74 7.236
13
P BND020 Bone Disease 59 6.764
14
URL001 Urolithiasis 46 6.691
15
P NRB001 Neuroblastoma 66 6.069
16
NPH009 Nephrolithiasis 54 6.018
17
P HRP006 Herpes Simplex 65 4.997
18
CHG001 Chagas Disease 66 4.997
19
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 4.899
20
MMM001 Mammary Paget's Disease 53 4.790
21
P NRP001 Neuropathy 60 4.748
22
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 4.603
23
OST159 Osteogenic Sarcoma 66 4.594
24
c ACT071 Acute Kidney Failure 60 4.573
25
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 49 4.538
26
ART002 Arts Syndrome 66 4.534
27
HLX001 Helix Syndrome 48 4.518
28
ALL029 Allergic Disease 59 4.443
29
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 4.418
31
P PRP019 Peripheral Nervous System Disease 58 4.291
32
48X005 48,xyyy 39 4.246
33
P SNS001 Sensorineural Hearing Loss 59 4.074
34
P HYP086 Hypothyroidism 69 4.065
35
GLL048 Glial Tumor 52 4.023
36
GLM045 Glioma 63 4.023
37
P MYC084 Mycobacterium Tuberculosis 1 68 3.957
38
DHY008 Dihydroxyadeninuria 24 3.943
39
P HYP265 Hypotonia 42 3.912
40
c BRN108 Branchiootic Syndrome 1 62 3.909
41
HMN044 Human Immunodeficiency Virus Type 1 78 3.907
42
P INF032 Infertility 57 3.900
43
P LKM062 Leukemia, Acute Lymphoblastic 69 3.803
44
HYP266 Hypoxia 57 3.791
45
c CHR408 Charcot-Marie-Tooth Disease, X-Linked Recessive, 5 43 3.733
46
MLR004 Malaria 80 3.651
47
47X002 47,xyy 48 3.582
48
NPH003 Nephrocalcinosis 49 3.476
49
P KLZ004 Kala-Azar 1 41 3.464
50
LSH001 Leishmaniasis 64 3.464
51
CHR121 Charcot-Marie-Tooth Neuropathy X Type 5 17 3.455
52
DFN002 Dfnx1 Nonsyndromic Hearing Loss and Deafness 8 3.455
53
c PCH010 Pachyonychia Congenita 3 43 3.394
54
P DYS154 Dystonia 64 3.393
55
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.391
56
P PNC035 Pancreatic Cancer 86 3.371
57
MYL069 Myeloma, Multiple 77 3.364
58
P LKM002 Leukemia 67 3.353
59
HYP066 Hyperglycemia 61 3.267
60
RPD005 Rapidly Involuting Congenital Hemangioma 46 3.252
61
DSS032 Disease by Infectious Agent 55 3.251
62
PST092 Posttransplant Acute Limbic Encephalitis 28 3.248
63
VCC001 Vaccinia 47 3.241
64
TRY001 Trypanosomiasis 50 3.239
65
P GLY013 Glycogen Storage Disease 60 3.235
66
P MYC008 Myocarditis 59 3.224
67
P HPT021 Hepatitis 69 3.219
68
P OPT006 Optic Nerve Disease 58 3.206
69
ANX004 Anoxia 40 3.189
70
CYT002 Cytokine Deficiency 43 3.180
71
HYP017 Hypophosphatemia 49 3.162
72
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 3.127
73
SQM006 Squamous Cell Carcinoma 60 3.124
74
PLR008 Pleurisy 50 3.092
75
P CLR023 Colorectal Cancer 100 3.058
76
P MYP004 Myopathy 67 3.046
77
GLB002 Glioblastoma 67 3.043
78
AGN016 Aging 54 2.915
79
INS024 Insulin-Like Growth Factor I 78 2.870
80
SPS057 Spasticity 42 2.859
81
P MLN007 Male Infertility 56 2.851
82
P GST053 Gastric Cancer 83 2.830
83
SVR004 Severe Combined Immunodeficiency 72 2.824
84
NPH091 Nephrolithiasis, Calcium Oxalate 61 2.822
85
CHL014 Cholera 62 2.777
86
OPT071 Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Recessive 18 2.765
87
ORL015 Oral Squamous Cell Carcinoma 43 2.701
88
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 2.692
89
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 2.675
90
P FBR017 Fibrosarcoma 56 2.671
91
CYS001 Cystic Fibrosis 78 2.635
92
c HPT073 Hepatitis C Virus 71 2.635
93
BRK010 Burkitt Lymphoma 66 2.613
94
P ENC018 Encephalopathy 62 2.587
95
P CHR071 Charcot-Marie-Tooth Disease 64 2.560
96
TTH006 Tooth Disease 51 2.560
97
P PRS040 Prostate Cancer 95 2.549
98
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 2.542
99
c HPT001 Hepatitis C 62 2.538
100
DWN001 Down Syndrome 70 2.534
101
c SCL052 Scleroderma, Familial Progressive 61 2.531
102
P SYS005 Systemic Scleroderma 74 2.487
103
P LKM071 Leukemia, Chronic Lymphocytic 75 2.475
104
CNN005 Connective Tissue Disease 67 2.395
105
BCT022 Bacterial Infectious Disease 56 2.379
106
SLP001 Sleeping Sickness 56 2.379
107
ORT008 Orotic Aciduria 57 2.337
108
P OVR042 Ovarian Cancer 88 2.329
109
FTT001 Fatty Liver Disease 62 2.317
110
SPP011 Suppression of Tumorigenicity 12 61 2.307
111
ACR007 Acromegaly 70 2.254
112
MYL009 Myelodysplastic Syndrome 67 2.233
113
IMM167 Immune Deficiency Disease 78 2.217
114
P BRS044 Breast Adenocarcinoma 58 2.206
115
P BLD134 Bladder Cancer 79 2.186
116
ATS010 Autosomal Recessive Disease 42 2.176
117
TRT001 Teratocarcinoma 42 2.175
118
P PHC003 Pheochromocytoma 69 2.164
119
ADR040 Adrenal Gland Pheochromocytoma 46 2.164
120
P INF038 Influenza 68 2.135
121
PRM329 Premature Aging 36 2.127
122
GTR002 Goiter 53 2.127
123
MSC007 Muscle Hypertrophy 64 2.122
124
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.122
125
c DNT047 Dentinogenesis Imperfecta Type 2 35 2.120
126
NRR001 Neuroretinitis 42 2.100
127
RTN023 Retinitis 46 2.100
128
c SYS001 Systemic Lupus Erythematosus 87 2.075
129
BRC012 Brucellosis 66 2.070
130
P INF037 Inflammatory Bowel Disease 53 2.063
131
ISC004 Ischemia 61 2.045
132
c DFN194 Deafness, X-Linked 1 35 2.041
133
PTT037 Pituitary Tumors 44 2.018
134
ACT098 Acute Erythroid Leukemia 55 2.016
135
P PRM002 Primary Hyperoxaluria 65 2.016
136
P LVR013 Liver Disease 69 2.014
137
c HYP794 Hyperoxaluria, Primary, Type I 63 1.998
138
DSS010 Dissociative Disorder 39 1.997
139
DGN001 Degenerative Disc Disease 49 1.997
140
SFT003 Soft Tissue Sarcoma 57 1.983
141
P OVR082 Overgrowth Syndrome 49 1.979
142
GRD001 Giardiasis 46 1.977
143
c HPT003 Hepatitis a 63 1.974
144
P MYS003 Myasthenia Gravis 68 1.946
145
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.943
146
ACT119 Acute Promyelocytic Leukemia 62 1.932
147
KDN013 Kidney Hypertrophy 34 1.932
148
ORL011 Oral Cancer 60 1.911
149
P ALZ034 Alzheimer Disease 87 1.910
150
ESP021 Esophageal Cancer 83 1.900
151
P CRD119 Cardiac Arrest 67 1.885
152
DYS073 Dysphagia 53 1.885
153
P LPS004 Lupus Erythematosus 61 1.876
154
CLR109 Colorectal Adenocarcinoma 50 1.872
155
SPN186 Spinal Cord Injury 61 1.855
156
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 1.798
157
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.775
158
P URN019 Urinary Tract Infection 49 1.775
159
MDD018 Middle East Respiratory Syndrome 44 1.775
160
P LTR001 Lateral Sclerosis 58 1.775
161
P TXP001 Toxoplasmosis 60 1.775
162
c ACT073 Acute Leukemia 58 1.774
163
P BRS047 Breast Cancer 98 1.773
164
P BNG032 Benign Mesothelioma 53 1.773
165
P ADN016 Adenocarcinoma 63 1.772
166
P NNS072 Nonsyndromic Hearing Loss 40 1.755
167
CHL065 Cholangiocarcinoma 58 1.728
168
INT079 Intrahepatic Cholangiocarcinoma 51 1.728
169
CMB007 Combined Immunodeficiency 57 1.712
170
P MLN008 Melanoma 76 1.708
171
c RNG015 Ring Chromosome 2 22 1.708
172
P PRD008 Periodontitis 64 1.702
173
P EXN002 Exanthem 58 1.687
174
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.687
175
c LKM005 Leukemia, T-Cell, Chronic 34 1.687
176
CYS013 Cystinuria 66 1.666
177
c CHR571 Charcot-Marie-Tooth Disease Type 5 23 1.666
178
MCS002 Mucositis 56 1.666
179
c INH020 Inherited Metabolic Disorder 48 1.666
180
c XLN110 X-Linked Charcot-Marie-Tooth Disease 31 1.666
181
OCL069 Ocular Motor Apraxia 57 1.665
182
ART016 Aortic Aneurysm 68 1.665
183
TTN003 Tetanus 65 1.665
184
WLS001 Wilson Disease 70 1.657
185
INS001 Insulinoma 59 1.643
186
P TRT010 Teratoma 51 1.643
187
PRT251 Proteinuria, Chronic Benign 57 1.586
188
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 1.586
189
QDR001 Quadriplegia 50 1.586
190
c LKM061 Leukemia, Acute Myeloid 83 1.583
191
P HNT016 Huntington Disease 73 1.583
192
P GLM040 Glioma Susceptibility 1 71 1.566
193
CRH001 Crohn's Disease 80 1.566
194
MLG169 Malignant Astrocytoma 57 1.566
195
STM007 Stomatitis 54 1.566
196
URT049 Urate Oxidase, Pseudogene 24 1.566
197
P NTR004 Neutropenia 63 1.543
198
ARG004 Argyria 26 1.510
199
EMB004 Embryonal Carcinoma 56 1.497
200
FSC004 Fasciitis 49 1.474
201
c ACT134 Acute Liver Failure 59 1.467
202
PLM010 Pulmonary Edema 55 1.467
203
c RNG021 Ring Chromosome 5 20 1.453
204
MTB004 Metabolic Acidosis 48 1.450
205
HMN047 Human Cytomegalovirus Infection 57 1.450
206
P ALC033 Alcohol Use Disorder 61 1.450
207
CHL123 Chlamydia 58 1.446
208
P LNG032 Lung Cancer 98 1.443
209
ATM095 Autoimmune Disease 61 1.443
210
LGN006 Legionnaire Disease 52 1.443
211
XLN244 X-Linked Sensorineural Deafness 15 1.443
212
DPH001 Diphtheria 59 1.443
213
ADN001 Adenosine Deaminase Deficiency 59 1.399
214
CND006 Candida Glabrata 30 1.398
215
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.376
216
c ACT068 Acute Cystitis 61 1.376
217
SRC014 Sarcoma 65 1.376
218
CYS010 Cystinosis 62 1.324
219
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 1.312
220
HYP141 Hyperphenylalaninemia 42 1.312
221
ANR040 Aneurysm 61 1.312
222
c INH030 Inherited Retinal Disorder 28 1.297
223
P LYM118 Lymphoma 67 1.297
224
P BCL017 B-Cell Lymphoma 59 1.297
225
FND002 Fundus Dystrophy 55 1.297
226
c MCR130 Microvascular Complications of Diabetes 6 41 1.296
227
c MCR120 Microvascular Complications of Diabetes 7 47 1.296
228
P SPP010 Suppressor of Tumorigenicity 3 51 1.296
229
ULC004 Ulcerative Colitis 74 1.296
230
P MYL006 Myeloid Leukemia 61 1.296
231
c MCR113 Microvascular Complications of Diabetes 3 52 1.296
232
c MCR133 Microvascular Complications of Diabetes 4 41 1.296
233
P DNG005 Dengue Virus 56 1.296
234
P APL001 Aplastic Anemia 73 1.291
235
P PLY014 Polycystic Kidney Disease 69 1.291
236
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.291
237
MLY001 Molybdenum Cofactor Deficiency 40 1.291
238
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 1.291
239
SKN016 Skin Disease 63 1.291
240
HGH043 High Grade Glioma 45 1.291
241
ATH004 Athetosis 25 1.291
242
P DBT005 Diabetes Insipidus 54 1.208
243
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.208
244
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.208
245
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.208
246
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 1.208
247
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 1.208
248
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.208
249
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 1.208
250
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.208
251
MYL005 Myelofibrosis 71 1.208
252
c SML038 Small Cell Cancer of the Lung 69 1.208
253
FBR009 Fibrous Dysplasia 48 1.208
254
c PLM127 Pulmonary Hypertension, Primary, 3 34 1.208
255
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.208
256
TXC005 Toxic Shock Syndrome 62 1.208
257
XLN174 X-Linked Non-Syndromic Sensorineural Deafness Type Dfn 20 1.178
258
c MJR022 Major Affective Disorder 8 38 1.178
259
KPS004 Kaposi Sarcoma 77 1.178
260
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.178
261
c MJR024 Major Affective Disorder 9 41 1.178
262
P BPL003 Bipolar Disorder 56 1.178
263
P LNG064 Lung Cancer Susceptibility 3 70 1.178
264
PPL022 Papilloma 53 1.178
265
SQM002 Squamous Cell Papilloma 46 1.178
266
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 1.178
267
P XNT004 Xanthinuria 37 1.168
268
MLY008 Molybdenum Cofactor Deficiency, Complementation Group a 47 1.168
270
TLN003 Telangiectasis 51 1.168
271
c HRD142 Hereditary Xanthinuria 43 1.168
272
PHR003 Pharyngitis 58 1.150
273
CRV035 Cervical Cancer 73 1.108
274
P PLM037 Pulmonary Hypertension 72 1.108
275
c PLM121 Pulmonary Hypertension, Primary, 4 28 1.108
276
PLS011 Plasmacytoma 56 1.108
277
KRT009 Keratosis 53 1.108
278
THY030 Thyroid Gland Disease 50 1.108
279
c TBL031 Tubulointerstitial Kidney Disease, Autosomal Dominant, 1 47 1.023
280
c SHR067 Short-Rib Thoracic Dysplasia 2 with or Without Polydactyly 44 1.023
281
CHL152 Childhood Acute Lymphocytic Leukemia 50 1.023
282
PRP001 Propionic Acidemia 65 1.023
283
CTR172 Citrullinemia, Classic 65 1.023
284
TRM010 Traumatic Brain Injury 51 1.023
285
P MTH008 Methylmalonic Acidemia 52 1.023
286
NRN001 Neuroendocrine Carcinoma 47 1.023
287
CRB004 Cerebral Artery Occlusion 45 1.023
288
P FNC004 Fanconi Syndrome 60 1.023
289
P ADL010 Adult Respiratory Distress Syndrome 71 1.023
290
ISL099 Isolated Methylmalonic Acidemia 36 1.023
291
P THL005 Thalassemia 56 0.988
292
P NSP012 Nasopharyngeal Carcinoma 61 0.988
293
RTN187 Retinitis Pigmentosa-Deafness Syndrome 48 0.988
294
P MLT020 Multiple Sclerosis 79 0.988
295
c BTT014 Beta-Thalassemia 72 0.988
296
DFF005 Diffuse Large B-Cell Lymphoma 54 0.988
297
P USH001 Usher Syndrome 64 0.988
298
LPT014 Leptin Deficiency or Dysfunction 78 0.988
299
P HPT023 Hepatocellular Carcinoma 96 0.988
300
RNL077 Renal Fibrosis 46 0.988
301
INT067 Interstitial Nephritis 46 0.988
302
VSC003 Visceral Leishmaniasis 55 0.988
303
c VRL010 Viral Hepatitis 53 0.988
304
P RTN016 Retinal Degeneration 52 0.988
305
c HPT016 Hepatitis B 62 0.988
306
P MTC069 Mitochondrial Disorders 57 0.988
307
P SCK005 Sickle Cell Disease 56 0.988
308
c AMY009 Amyloidosis Aa 47 0.988
309
P RTN008 Retinitis Pigmentosa 80 0.833
310
P NRP066 Neuropathy, Hereditary Motor and Sensory, Type Via, with Optic Atrophy 42 0.833
311
c ALP101 Alpha-Thalassemia 62 0.833
312
P PRK057 Parkinson Disease, Late-Onset 80 0.833
313
CHR100 Chronic Ulcer of Skin 57 0.833
314
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.833
315
P PRM293 Primary Mediastinal B-Cell Lymphoma 43 0.833
316
NPH113 Nephroma 37 0.833
317
THL010 Thalassemia Minor 32 0.833
318
c XLN004 X-Linked Nonsyndromic Deafness 28 0.833
319
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 43 0.833
320
P THP004 Thiopurines, Poor Metabolism of, 1 42 0.833
321
PLY001 Polycythemia Vera 69 0.833
322
CLB010 Coloboma of Macula 53 0.833
323
NLP001 Nail-Patella Syndrome 63 0.833
324
HRD224 Hereditary Nonpolyposis Colon Cancer 51 0.833
325
RLP008 Relapsed/refractory Diffuse Large B-Cell Lymphoma 31 0.833
326
P MVM001 Movement Disease 61 0.833
327
P HML002 Hemolytic Anemia 62 0.833
328
HPT022 Hepatoblastoma 54 0.833
329
P SKN015 Skin Carcinoma 71 0.833
330
P CND004 Candidiasis 58 0.833
331
P LYN001 Lynch Syndrome 76 0.833
332
P THY032 Thyroiditis 57 0.833
333
P PLY018 Polycythemia 56 0.833
334
P GRF003 Graft-Versus-Host Disease 71 0.833
335
SYN005 Synostosis 43 0.833
336
P NPH005 Nephronophthisis 56 0.833
337
CCC002 Coccidiosis 50 0.833
338
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 0.833
339
BRN024 Bronchitis 67 0.833
340
P CYS039 Cystic Kidney Disease 53 0.833
341
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.833
342
NWC001 Newcastle Disease 47 0.833
343
NRM004 Neuroma 49 0.833
344
c NNS007 Nonsyndromic Deafness 33 0.833
345
RYN005 Raynaud Phenomenon 45 0.833
346
c ATM075 Autoimmune Encephalitis 40 0.833
347
MSL001 Measles 61 0.833
348
MYC015 Mycobacterium Fortuitum 28 0.833
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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