Search results for Histidine

727 hits were found for Histidine

# Family MCID Name MIFTS Score
1
HST006 Histidinemia 49 5.416
2
THR120 Thrombophilia Due to Histidine-Rich Glycoprotein Deficiency 23 5.300
3
HST007 Histidine Metabolism Disease 23 5.230
4
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.715
5
HLX001 Helix Syndrome 46 0.220
6
48X005 48,xyyy 37 0.151
7
MST004 Mast Cell Neoplasm 40 0.144
8
EXT007 Extracutaneous Mastocytoma 39 0.144
9
MNK001 Menkes Disease 62 0.141
10
MLR004 Malaria 82 0.136
11
P LNG032 Lung Cancer 99 0.113
12
SQM006 Squamous Cell Carcinoma 60 0.104
13
PLS007 Plasmodium Falciparum Malaria 53 0.104
14
CRV035 Cervical Cancer 77 0.100
15
P CLR023 Colorectal Cancer 100 0.096
16
P KDN018 Kidney Disease 73 0.096
17
P ADN016 Adenocarcinoma 65 0.096
18
P CTR002 Cataract 62 0.096
19
P HPT023 Hepatocellular Carcinoma 99 0.093
20
P BRS047 Breast Cancer 99 0.093
21
P RHM011 Rheumatoid Arthritis 82 0.093
22
P SZR006 Seizure Disorder 59 0.093
23
VSL002 Visual Epilepsy 58 0.093
24
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.093
25
P GST053 Gastric Cancer 85 0.089
26
PRT037 Pertussis 66 0.089
27
DPH001 Diphtheria 61 0.089
28
P GST044 Gastritis 58 0.089
29
HMP009 Haemophilus Influenzae 46 0.089
30
c RNG015 Ring Chromosome 2 27 0.089
31
P CRD119 Cardiac Arrest 71 0.085
32
P NRB010 Neuroblastoma 1 66 0.085
33
47X002 47,xyy 49 0.085
34
LVR012 Liver Cirrhosis 67 0.080
35
GLL008 Gilles De La Tourette Syndrome 66 0.080
36
P ENC018 Encephalopathy 64 0.080
37
ISC004 Ischemia 62 0.080
38
ADN018 Adenoma 60 0.080
39
PPL052 Papillomatosis, Confluent and Reticulated 34 0.080
40
P ALZ034 Alzheimer Disease 90 0.076
41
ESP021 Esophageal Cancer 90 0.076
42
c SML038 Small Cell Cancer of the Lung 67 0.076
43
MST024 Mastocytosis, Cutaneous 65 0.076
44
c PRC016 Pre-Eclampsia 63 0.076
45
ATM095 Autoimmune Disease 62 0.076
46
CHL014 Cholera 58 0.076
47
VCC001 Vaccinia 50 0.076
48
c CRV002 Cervix Uteri Carcinoma in Situ 47 0.076
49
CYT002 Cytokine Deficiency 46 0.076
50
CRV045 Cervical Intraepithelial Neoplasia 41 0.076
51
HST019 Histidinuria Due to a Renal Tubular Defect 13 0.076
52
c HYP836 Hypercholesterolemia, Familial, 1 74 0.071
53
P LVR013 Liver Disease 71 0.071
54
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.071
55
PPT005 Peptic Ulcer Disease 60 0.071
56
BCT022 Bacterial Infectious Disease 57 0.071
57
OCL069 Ocular Motor Apraxia 53 0.071
58
P THR015 Thrombophilia 51 0.071
59
c ATS307 Autosomal Recessive Cerebellar Ataxia 44 0.071
60
HRW001 Hair Whorl 36 0.071
61
P HRT032 Heart Disease 78 0.065
62
P PRD008 Periodontitis 66 0.065
63
ALL026 Allergic Hypersensitivity Disease 65 0.065
64
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.065
65
P URT039 Urticaria 61 0.065
66
THR024 Thrombosis 58 0.065
67
PRT038 Protein-Energy Malnutrition 56 0.065
68
P DRR001 Diarrhea 55 0.065
69
STM007 Stomatitis 51 0.065
70
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.065
71
HPT004 Hepatic Coma 42 0.065
72
GLT005 Glutamate Formiminotransferase Deficiency 35 0.065
73
ARG004 Argyria 28 0.065
74
URC006 Urocanase Deficiency 25 0.065
75
c ERY064 Erythrocytosis, Familial, 6 22 0.065
76
P OVR042 Ovarian Cancer 89 0.060
77
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.060
78
c DLT002 Dilated Cardiomyopathy 81 0.060
79
ANX010 Anxiety 75 0.060
80
c THR092 Thrombophilia Due to Thrombin Defect 74 0.060
81
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.060
82
SVR004 Severe Combined Immunodeficiency 74 0.060
83
HMN044 Human Immunodeficiency Virus Type 1 73 0.060
84
P ART022 Arthritis 71 0.060
85
CHL065 Cholangiocarcinoma 68 0.060
86
ATH013 Atherosclerosis Susceptibility 68 0.060
87
MLN008 Melanoma 68 0.060
88
P DRM053 Dermatitis, Atopic 68 0.060
89
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.060
90
GST040 Gastric Adenocarcinoma 67 0.060
91
P HRP006 Herpes Simplex 66 0.060
92
DRM006 Dermatitis 63 0.060
93
TXC005 Toxic Shock Syndrome 63 0.060
94
HPT019 Hepatic Encephalopathy 60 0.060
95
P INF037 Inflammatory Bowel Disease 57 0.060
96
P FBR017 Fibrosarcoma 57 0.060
97
BRN004 Brain Edema 57 0.060
98
ANT024 Anthrax Disease 56 0.060
99
INT079 Intrahepatic Cholangiocarcinoma 54 0.060
100
SPP010 Suppressor of Tumorigenicity 3 54 0.060
101
c ACT134 Acute Liver Failure 53 0.060
102
OCC006 Occipital Horn Syndrome 51 0.060
103
PST092 Posttransplant Acute Limbic Encephalitis 29 0.060
104
P PRS040 Prostate Cancer 97 0.053
106
P PRK057 Parkinson Disease, Late-Onset 77 0.053
107
ULC004 Ulcerative Colitis 75 0.053
108
c HPT073 Hepatitis C Virus 74 0.053
109
P AMY004 Amyloidosis 71 0.053
110
P PHC003 Pheochromocytoma 71 0.053
111
P INF038 Influenza 69 0.053
112
CNG034 Congestive Heart Failure 69 0.053
113
ALL003 Allergic Rhinitis 69 0.053
114
HYP056 Hypoglycemia 68 0.053
115
P HML002 Hemolytic Anemia 64 0.053
116
P MST009 Mastocytosis 62 0.053
117
TTN003 Tetanus 62 0.053
118
HLC007 Helicobacter Pylori Infection 61 0.053
119
INS001 Insulinoma 60 0.053
120
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.053
121
P CRN300 Coronary Heart Disease 1 59 0.053
122
P RHN004 Rhinitis 59 0.053
123
EYD002 Eye Disease 59 0.053
124
c ACT075 Acute Myocardial Infarction 59 0.053
125
CRV038 Cervical Squamous Cell Carcinoma 58 0.053
126
P DNG005 Dengue Virus 57 0.053
127
HYP060 Hyperinsulinism 55 0.053
128
MST005 Mastitis 55 0.053
129
P HYP076 Hyperthyroidism 55 0.053
130
STT041 Stuttering 53 0.053
131
URM002 Uremia 50 0.053
132
KWS001 Kwashiorkor 46 0.053
133
MYL069 Myeloma, Multiple 85 0.046
134
OST012 Osteoarthritis 80 0.046
135
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.046
136
P RTN008 Retinitis Pigmentosa 77 0.046
137
DFC004 Deficiency Anemia 77 0.046
138
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.046
139
P MYC007 Myocardial Infarction 74 0.046
140
PHN003 Phenylketonuria 73 0.046
141
P HNT016 Huntington Disease 72 0.046
142
ACR007 Acromegaly 70 0.046
143
c CHR684 Chronic Kidney Disease 68 0.046
144
P LKM062 Leukemia, Acute Lymphoblastic 68 0.046
145
P NSP012 Nasopharyngeal Carcinoma 67 0.046
146
P HYP098 Hypereosinophilic Syndrome 67 0.046
147
P ASP006 Aspergillosis 67 0.046
148
P PLM036 Pulmonary Fibrosis 66 0.046
149
P TRN020 Turner Syndrome 66 0.046
150
IDP011 Idiopathic Interstitial Pneumonia 65 0.046
151
CLR108 Colorectal Adenoma 64 0.046
152
c FNC043 Fanconi Anemia, Complementation Group E 64 0.046
153
P ENC004 Encephalitis 64 0.046
154
P GLM045 Glioma 64 0.046
155
P PSR002 Psoriasis 63 0.046
156
CLT003 Colitis 63 0.046
157
HYP066 Hyperglycemia 63 0.046
158
FTT001 Fatty Liver Disease 63 0.046
159
P CND004 Candidiasis 61 0.046
160
c ACT071 Acute Kidney Failure 60 0.046
161
P KDN017 Kidney Cancer 60 0.046
162
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 60 0.046
163
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.046
164
c ACT210 Acute Respiratory Distress Syndrome 59 0.046
165
NWB001 Newborn Respiratory Distress Syndrome 58 0.046
166
P HMP007 Hemophilia 58 0.046
167
HYP266 Hypoxia 58 0.046
168
CNT047 Contact Dermatitis 58 0.046
169
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.046
170
AGN016 Aging 58 0.046
171
P NRP001 Neuropathy 57 0.046
172
P LYM031 Lymphocytic Leukemia 56 0.046
173
P PLY018 Polycythemia 56 0.046
174
P RTN016 Retinal Degeneration 56 0.046
175
P TCD001 Tic Disorder 55 0.046
176
P SML001 Small Cell Carcinoma 55 0.046
177
TRM010 Traumatic Brain Injury 54 0.046
178
BNR002 Bone Resorption Disease 51 0.046
179
ADR040 Adrenal Gland Pheochromocytoma 51 0.046
180
PST011 Pustulosis of Palm and Sole 51 0.046
181
CRC014 Carcinoid Tumors, Intestinal 49 0.046
182
RTN023 Retinitis 46 0.046
183
NRR001 Neuroretinitis 46 0.046
184
ORL015 Oral Squamous Cell Carcinoma 44 0.046
185
P DYS026 Dysfibrinogenemia 42 0.046
186
PYR021 Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency 38 0.046
187
DSR031 Disorder of Copper Metabolism 29 0.046
188
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.038
189
c SYS001 Systemic Lupus Erythematosus 88 0.038
190
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.038
191
c HYP595 Hypertension, Essential 87 0.038
192
CYS001 Cystic Fibrosis 84 0.038
193
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.038
194
AST005 Asthma 80 0.038
195
INS024 Insulin-Like Growth Factor I 79 0.038
196
P BLD134 Bladder Cancer 79 0.038
197
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.038
198
GST019 Gastrointestinal Stromal Tumor 76 0.038
199
c ATR087 Atrial Standstill 1 76 0.038
200
CRH001 Crohn's Disease 75 0.038
201
GLB002 Glioblastoma 74 0.038
202
c BTT014 Beta-Thalassemia 73 0.038
203
PLM001 Pulmonary Tuberculosis 72 0.038
204
MYL009 Myelodysplastic Syndrome 72 0.038
205
OTT002 Otitis Media 71 0.038
206
DWN001 Down Syndrome 70 0.038
207
P MYC084 Mycobacterium Tuberculosis 1 69 0.038
208
P LKM002 Leukemia 69 0.038
209
PNC129 Pancreatic Adenocarcinoma 69 0.038
210
SRC014 Sarcoma 67 0.038
211
P SKN015 Skin Carcinoma 67 0.038
212
P DBT009 Diabetes Mellitus 66 0.038
213
PRT036 Peritonitis 66 0.038
214
c HMP004 Hemophilia B 66 0.038
215
MLD001 Melioidosis 66 0.038
216
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.038
217
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.038
218
P VSC007 Vascular Disease 65 0.038
219
TBC004 Tobacco Addiction 65 0.038
220
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.038
221
P PRP019 Peripheral Nervous System Disease 64 0.038
222
ANR007 Anorexia Nervosa 64 0.038
223
LSH001 Leishmaniasis 64 0.038
224
c ACT068 Acute Cystitis 63 0.038
225
c HPT016 Hepatitis B 63 0.038
226
LYS012 Lysosomal Acid Lipase Deficiency 63 0.038
227
c SYS004 Systemic Mastocytosis 63 0.038
228
GLC006 Galactosemia 63 0.038
229
HYP020 Hyperprolactinemia 62 0.038
230
P RHB003 Rhabdomyosarcoma 62 0.038
231
LNG099 Lung Disease 62 0.038
232
BRC012 Brucellosis 62 0.038
233
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.038
234
c HPT001 Hepatitis C 62 0.038
235
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.038
236
CRC021 Carcinosarcoma 62 0.038
237
c SCL052 Scleroderma, Familial Progressive 62 0.038
238
THY029 Thyroid Carcinoma 62 0.038
239
P BCL017 B-Cell Lymphoma 61 0.038
240
NTR005 Nutritional Deficiency Disease 61 0.038
241
MSL001 Measles 61 0.038
242
P PNC044 Pancreatitis 61 0.038
243
P ADL010 Adult Respiratory Distress Syndrome 61 0.038
244
GLB015 Glioblastoma Multiforme 60 0.038
245
c ACT027 Acute Pancreatitis 60 0.038
246
P CTS001 Cutis Laxa 60 0.038
247
P EHL001 Ehlers-Danlos Syndrome 60 0.038
248
P INF032 Infertility 60 0.038
249
NRN004 Neuroendocrine Tumor 59 0.038
250
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.038
251
MRT001 Muir-Torre Syndrome 58 0.038
252
P PRP029 Porphyria 58 0.038
253
YLL002 Yellow Fever 58 0.038
254
IRN002 Iron Metabolism Disease 58 0.038
255
ERY051 Erythroleukemia, Familial 58 0.038
256
P TRC086 Trichohepatoenteric Syndrome 1 57 0.038
257
SCH014 Schistosomiasis 57 0.038
258
P PRN023 Prion Disease 57 0.038
259
HMG005 Hemoglobinopathy 57 0.038
260
SPN035 Spindle Cell Sarcoma 57 0.038
261
ALL006 Allergic Asthma 56 0.038
262
P ANT006 Antiphospholipid Syndrome 56 0.038
263
PPL022 Papilloma 56 0.038
264
P ART021 Arteriosclerosis 56 0.038
265
P LTR001 Lateral Sclerosis 56 0.038
266
WST005 West Nile Virus 56 0.038
267
GLC003 Glucose Intolerance 55 0.038
268
P PLY019 Polyneuropathy 55 0.038
269
c GRV008 Graves Disease 1 55 0.038
270
PRS045 Prostatic Hypertrophy 55 0.038
271
PRP016 Paraplegia 54 0.038
272
P RCT021 Rectum Cancer 54 0.038
273
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 54 0.038
274
CLR030 Clear Cell Renal Cell Carcinoma 54 0.038
275
DFF036 Differentiated Thyroid Carcinoma 53 0.038
276
P ECL001 Eclampsia 53 0.038
277
LNG031 Lung Benign Neoplasm 52 0.038
278
PRS021 Prostatic Adenoma 52 0.038
279
GSG001 Gas Gangrene 52 0.038
280
c INH020 Inherited Metabolic Disorder 51 0.038
281
P RTN022 Retinal Vein Occlusion 50 0.038
282
APR001 Apraxia 50 0.038
283
PRS129 Prostatic Hyperplasia, Benign 49 0.038
284
P ATR005 Atrophic Gastritis 49 0.038
285
SQM002 Squamous Cell Papilloma 49 0.038
286
SPL018 Splenomegaly 48 0.038
287
c CNT016 Central Retinal Vein Occlusion 48 0.038
288
INT078 Intracranial Thrombosis 48 0.038
289
LGN006 Legionnaire Disease 48 0.038
290
NRN001 Neuroendocrine Carcinoma 48 0.038
291
GLL048 Glial Tumor 48 0.038
292
c THY112 Thyroid Hormone Resistance, Generalized, Autosomal Dominant 46 0.038
293
P SMK004 Smoking As a Quantitative Trait Locus 3 46 0.038
294
P GNG009 Gangliosidosis 45 0.038
295
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.038
296
c PCH010 Pachyonychia Congenita 3 43 0.038
297
P HYP265 Hypotonia 43 0.038
298
RST023 Resting Heart Rate, Variation in 43 0.038
299
P KLZ004 Kala-Azar 1 43 0.038
300
SNL007 Senile Cataract 41 0.038
301
P BRB001 Beriberi 41 0.038
302
OCL015 Oculomotor Apraxia 40 0.038
303
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.038
304
CRB004 Cerebral Artery Occlusion 38 0.038
305
DNT008 Denture Stomatitis 38 0.038
306
HYP110 Hyperproinsulinemia 38 0.038
307
SCR011 Scrapie 37 0.038
308
HMN002 Human Granulocytic Anaplasmosis 35 0.038
309
ACR005 Acrodermatitis 35 0.038
310
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.038
311
PLY150 Polykaryocytosis Inducer 31 0.038
312
PYR016 Pyridoxine Deficiency 31 0.038
313
ENT007 Enteropathica 27 0.038
314
ART109 Arterial Thoracic Outlet Syndrome 23 0.038
315
HMG009 Hemoglobin Zurich 22 0.038
316
CHL098 Childhood Myocerebrohepatopathy Spectrum 20 0.038
317
P PNC035 Pancreatic Cancer 86 0.027
318
c LKM061 Leukemia, Acute Myeloid 84 0.027
319
P ATX030 Ataxia-Telangiectasia 83 0.027
320
c LKM071 Leukemia, Chronic Lymphocytic 81 0.027
321
IMM167 Immune Deficiency Disease 79 0.027
322
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.027
323
P SCH015 Schizophrenia 76 0.027
324
KPS004 Kaposi Sarcoma 75 0.027
325
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.027
326
END057 Endometrial Cancer 74 0.027
327
P RTN024 Retinoblastoma 74 0.027
328
P EPL164 Epilepsy 73 0.027
329
P MLT020 Multiple Sclerosis 73 0.027
330
P FML011 Familial Adenomatous Polyposis 73 0.027
331
VNH007 Von Hippel-Lindau Syndrome 73 0.027
332
P CNR004 Cone-Rod Dystrophy 2 72 0.027
333
P SRC025 Sarcoidosis 1 72 0.027
334
P GRF003 Graft-Versus-Host Disease 71 0.027
335
ART016 Aortic Aneurysm 71 0.027
336
c MGR028 Migraine with or Without Aura 1 70 0.027
337
P TTR001 Tetralogy of Fallot 70 0.027
338
PTZ001 Peutz-Jeghers Syndrome 70 0.027
339
P HYP086 Hypothyroidism 70 0.027
340
FRN006 Frontotemporal Dementia 70 0.027
341
LYM133 Lymphoma, Hodgkin, Classic 70 0.027
342
WLS001 Wilson Disease 69 0.027
343
P PLM037 Pulmonary Hypertension 69 0.027
344
P HPT021 Hepatitis 69 0.027
345
P CHR012 Chronic Granulomatous Disease 69 0.027
346
c HMP029 Hemophilia a 69 0.027
347
P SYS005 Systemic Scleroderma 68 0.027
348
P DMN002 Dementia 68 0.027
349
GST092 Gastroesophageal Reflux 68 0.027
350
P TYS001 Tay-Sachs Disease 68 0.027
351
BRK010 Burkitt Lymphoma 68 0.027
352
P MCR115 Microvascular Complications of Diabetes 5 67 0.027
353
P CRN018 Coronary Artery Anomaly 67 0.027
354
P CNJ013 Conjunctivitis 67 0.027
355
PRT010 Parathyroid Carcinoma 67 0.027
356
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.027
357
P THR014 Thrombocytopenia 67 0.027
358
P MNN013 Meningitis 67 0.027
359
OST159 Osteogenic Sarcoma 67 0.027
360
P PRP003 Porphyria Cutanea Tarda 66 0.027
361
AND002 Androgen Insensitivity Syndrome 66 0.027
362
CHG001 Chagas Disease 66 0.027
363
P MTR014 Motor Neuron Disease 66 0.027
364
FML089 Familial Thoracic Aortic Aneurysm and Dissection 65 0.027
365
c GCH015 Gaucher Disease, Type I 65 0.027
366
OST017 Osteomyelitis 65 0.027
367
MSC007 Muscle Hypertrophy 65 0.027
368
P HYP069 Hyperparathyroidism 64 0.027
369
P VSC011 Vasculitis 64 0.027
370
SKN016 Skin Disease 64 0.027
371
HMT002 Hematologic Cancer 64 0.027
372
LPD008 Lipid Metabolism Disorder 64 0.027
373
P ANR048 Aniridia 1 64 0.027
374
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.027
375
P GCH001 Gaucher's Disease 63 0.027
376
GT001 Gout 63 0.027
377
PSR001 Psoriatic Arthritis 63 0.027
378
P END044 Endometriosis 63 0.027
379
BRS099 Breast Ductal Carcinoma 63 0.027
380
SPN186 Spinal Cord Injury 63 0.027
381
MDD011 Mood Disorder 62 0.027
382
ADL002 Adult Syndrome 62 0.027
383
BLD131 Bladder Urothelial Carcinoma 62 0.027
384
c BRN108 Branchiootic Syndrome 1 62 0.027
385
P HMN010 Hemangioma 62 0.027
386
OST003 Osteonecrosis 62 0.027
387
P THL005 Thalassemia 62 0.027
388
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.027
389
VRL011 Viral Infectious Disease 62 0.027
390
PRP083 Porphyria, Acute Intermittent 62 0.027
391
TRN015 Transient Cerebral Ischemia 62 0.027
392
P ART067 Aortic Aneurysm, Familial Thoracic 1 62 0.027
393
ACN002 Acanthosis Nigricans 62 0.027
394
ORL011 Oral Cancer 62 0.027
395
P DRM010 Dermatomyositis 62 0.027
396
CRD223 Cardiac Arrhythmia 61 0.027
397
PTT048 Pituitary Adenoma, Prolactin-Secreting 61 0.027
398
CHL068 Cholestasis 61 0.027
399
c PNS012 Paine Syndrome 61 0.027
400
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.027
401
LKD001 Leukodystrophy 61 0.027
402
c MCP047 Mucopolysaccharidosis, Type Iva 61 0.027
403
CTN007 Cutaneous Leishmaniasis 61 0.027
404
ACQ007 Acquired Immunodeficiency Syndrome 61 0.027
405
P TXP001 Toxoplasmosis 61 0.027
406
P PLY014 Polycystic Kidney Disease 61 0.027
407
VRC005 Varicose Veins 61 0.027
408
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 61 0.027
409
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.027
410
P VNT002 Ventricular Septal Defect 61 0.027
411
GNG013 Gingivitis 60 0.027
412
CHL067 Cholecystitis 60 0.027
413
PRT058 Pure Autonomic Failure 60 0.027
414
ANR040 Aneurysm 60 0.027
415
CHL123 Chlamydia 60 0.027
416
P PRM002 Primary Hyperoxaluria 60 0.027
417
P PRD006 Prader-Willi Syndrome 60 0.027
418
PLM033 Pulmonary Embolism 60 0.027
419
ART140 Arteries, Anomalies of 60 0.027
420
END030 End Stage Renal Failure 60 0.027
421
c HPT003 Hepatitis a 60 0.027
422
P INT070 Intestinal Obstruction 60 0.027
423
c DWL002 Dowling-Degos Disease 1 59 0.027
424
P CYS018 Cystitis 59 0.027
425
RNL024 Renal Glucosuria 59 0.027
426
P HRD011 Hereditary Spherocytosis 59 0.027
427
c HRD002 Hereditary Angioedema 59 0.027
428
P BRS044 Breast Adenocarcinoma 59 0.027
429
P HDC001 Headache 59 0.027
430
c PRG047 Progressive Familial Intrahepatic Cholestasis 59 0.027
431
BRS051 Breast Disease 59 0.027
432
DNH001 Donohue Syndrome 59 0.027
434
c GM1007 Gm1 Gangliosidosis 59 0.027
435
P LRY044 Larynx Cancer 59 0.027
436
DBT087 Diabetes Insipidus, Neurohypophyseal 59 0.027
437
P UVT001 Uveitis 58 0.027
438
CHR177 Chromophobe Renal Cell Carcinoma 58 0.027
439
CYT008 Cytomegalovirus Infection 58 0.027
440
c GM1004 Gm1-Gangliosidosis, Type I 58 0.027
441
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.027
442
RBS001 Rabies 57 0.027
443
BRN045 Brunner Syndrome 57 0.027
444
GST050 Gastrointestinal System Disease 57 0.027
445
CPR004 Coproporphyria, Hereditary 57 0.027
446
EMB004 Embryonal Carcinoma 57 0.027
447
GLL018 Gallbladder Cancer 57 0.027
448
P MLN007 Male Infertility 57 0.027
449
VSC002 Vascular Dementia 57 0.027
450
c ANG068 Angioedema, Hereditary, Type I 57 0.027
451
ANT009 Antithrombin Iii Deficiency 57 0.027
452
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.027
453
RHM027 Rheumatic Disease 56 0.027
454
ACT200 Acute Monoblastic Leukemia 56 0.027
455
PRP030 Purpura 56 0.027
456
ALL010 Allergic Contact Dermatitis 56 0.027
457
CLL003 Cellulitis 56 0.027
458
CRH005 Crohn's Colitis 56 0.027
459
P RBL001 Rubella 56 0.027
460
c VRL010 Viral Hepatitis 56 0.027
461
P SCK002 Sick Sinus Syndrome 56 0.027
462
c SVR001 Severe Acute Respiratory Syndrome 56 0.027
463
AND020 Androgen Insensitivity, Partial 56 0.027
464
JPN002 Japanese Encephalitis 56 0.027
465
MTH009 Mouth Disease 56 0.027
466
c PRD040 Periodontitis, Chronic 56 0.027
467
CNV004 Canavan Disease 56 0.027
468
RHM001 Rheumatic Fever 56 0.027
469
P NRC002 Narcolepsy 56 0.027
470
P INT068 Intestinal Disease 56 0.027
471
PLM010 Pulmonary Edema 56 0.027
472
HRT012 Heart Valve Disease 56 0.027
473
P SBS003 Substance Abuse 56 0.027
474
c MTC056 Mitochondrial Dna Depletion Syndrome 4a 55 0.027
475
c MCR113 Microvascular Complications of Diabetes 3 55 0.027
476
c SPN294 Spinocerebellar Ataxia 1 55 0.027
477
ADN027 Adenomyosis 55 0.027
478
PRC002 Paracoccidioidomycosis 55 0.027
479
VSC003 Visceral Leishmaniasis 55 0.027
480
c LKM070 Leukemia, Acute Monocytic 55 0.027
481
PRP082 Porphyria, Congenital Erythropoietic 55 0.027
482
P INS002 in Situ Carcinoma 55 0.027
483
P OVR049 Ovarian Disease 55 0.027
484
P HST010 Histiocytosis 54 0.027
485
OVR059 Ovary Adenocarcinoma 54 0.027
486
c ACT020 Acute T Cell Leukemia 54 0.027
487
GNT003 Genital Herpes 54 0.027
488
FCT001 Factor Viii Deficiency 54 0.027
489
P ANG015 Angioedema 54 0.027
490
P HYP050 Hyperinsulinemic Hypoglycemia 54 0.027
491
P DBT005 Diabetes Insipidus 54 0.027
492
LYM040 Lymphoblastic Lymphoma 54 0.027
493
PLM017 Pulmonary Alveolar Microlithiasis 54 0.027
494
ECH003 Echinococcosis 54 0.027
495
RSP002 Respiratory Syncytial Virus Infectious Disease 54 0.027
496
TLN003 Telangiectasis 53 0.027
497
VLV032 Vulva Cancer 53 0.027
498
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.027
499
P CHL066 Cholangitis 53 0.027
500
TCK001 Tick-Borne Encephalitis 53 0.027
501
P RTN018 Retinal Disease 53 0.027
502
P MGR003 Migraine with Aura 53 0.027
503
GST023 Gastric Ulcer 53 0.027
504
c OST163 Osteopetrosis, Autosomal Recessive 3 53 0.027
505
MCP006 Mucoepidermoid Carcinoma 53 0.027
506
c ACT135 Acute Graft Versus Host Disease 52 0.027
507
c PST005 Posterior Uveitis 52 0.027
508
RTN003 Retinal Ischemia 52 0.027
509
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.027
510
DNT012 Dental Caries 52 0.027
511
c MYS033 Miyoshi Muscular Dystrophy 1 52 0.027
512
PNG002 Pain Agnosia 52 0.027
513
P MNC007 Monocytic Leukemia 52 0.027
514
c SCN007 Secondary Hyperparathyroidism 52 0.027
515
P CTN015 Cutaneous T Cell Lymphoma 52 0.027
516
P CPL006 Capillary Hemangioma 52 0.027
517
P TRT010 Teratoma 52 0.027
518
PRT029 Parathyroid Adenoma 52 0.027
519
MCL006 Macular Retinal Edema 52 0.027
520
P CHR345 Chronic Pain 52 0.027
521
P RNL017 Renal Oncocytoma 52 0.027
522
P AST007 Astrocytoma 52 0.027
523
HRT011 Heart Septal Defect 52 0.027
524
P MSC003 Muscular Atrophy 52 0.027
525
PLC008 Placenta Disease 51 0.027
526
c MLG054 Malignant Histiocytosis 51 0.027
527
PRN011 Pernicious Anemia 51 0.027
528
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.027
529
CLR109 Colorectal Adenocarcinoma 51 0.027
530
GLS018 Glass Syndrome 51 0.027
531
HYP063 Hypersplenism 51 0.027
532
ALL001 Allan-Herndon-Dudley Syndrome 50 0.027
533
CRY003 Cryptosporidiosis 50 0.027
534
P DDN001 Duodenal Ulcer 50 0.027
535
SCB001 Scabies 50 0.027
536
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.027
537
ACR041 Acromelic Frontonasal Dysostosis 50 0.027
538
P SHR001 Short Bowel Syndrome 50 0.027
539
P PNV001 Panuveitis 50 0.027
540
ALV002 Alveolar Echinococcosis 50 0.027
541
STM006 Stomach Disease 50 0.027
542
RFR010 Refractory Anemia 50 0.027
543
MCR004 Macroglobulinemia 50 0.027
544
ALL009 Allergic Conjunctivitis 50 0.027
545
ALN001 Aland Island Eye Disease 50 0.027
546
THR016 Thrombophlebitis 50 0.027
547
CRN030 Coronary Stenosis 49 0.027
548
ESP002 Esophageal Varix 49 0.027
549
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.027
550
c MTR002 Mitral Valve Insufficiency 49 0.027
551
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 49 0.027
552
P FML355 Familial Intrahepatic Cholestasis 49 0.027
553
c BCT013 Bacterial Pneumonia 49 0.027
554
ENC055 Encephalopathy, Ethylmalonic 49 0.027
555
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.027
556
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.027
557
P CRV031 Cervical Adenocarcinoma 49 0.027
558
HPR003 Heparin-Induced Thrombocytopenia 49 0.027
559
c HPT015 Hepatitis D 49 0.027
560
THR013 Thoracic Outlet Syndrome 49 0.027
561
P BRS053 Breast Fibroadenoma 49 0.027
562
c INV001 Invasive Aspergillosis 48 0.027
563
MTB004 Metabolic Acidosis 48 0.027
564
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.027
565
c MCR120 Microvascular Complications of Diabetes 7 48 0.027
566
CRN027 Corneal Neovascularization 48 0.027
567
PRM020 Premenstrual Tension 48 0.027
568
LYM019 Lymphosarcoma 48 0.027
569
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.027
570
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.027
571
ALB002 Albinism 48 0.027
572
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.027
573
PLP001 Pulpitis 48 0.027
574
WTH001 Withdrawal Disorder 47 0.027
575
HRT031 Hartnup Disorder 47 0.027
576
P MGR001 Migraine Without Aura 47 0.027
577
P HMR005 Hemorrhoid 47 0.027
578
NSS002 Neisseria Meningitidis Infection 47 0.027
579
AML029 Ameloblastoma 47 0.027
580
PTT037 Pituitary Tumors 47 0.027
581
CRY004 Cryoglobulinemia 47 0.027
583
P MYC033 Myoclonus 47 0.027
584
VPM001 Vipoma 47 0.027
585
3HY007 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency 47 0.027
586
NCR007 Necrotizing Fasciitis 47 0.027
587
P BNG032 Benign Mesothelioma 47 0.027
588
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.027
589
FSC004 Fasciitis 47 0.027
590
P MTH007 Methemoglobinemia 47 0.027
591
MCL027 Macular Dystrophy, Dominant Cystoid 47 0.027
592
P SDR003 Sideroblastic Anemia 47 0.027
593
DBT006 Diabetic Macular Edema 46 0.027
594
SNT005 Sinoatrial Node Disease 46 0.027
595
MNN020 Meningococcal Infection 46 0.027
596
ZKF001 Zika Fever 46 0.027
597
MCR018 Microcytic Anemia 46 0.027
598
c MLG068 Malignant Glioma 46 0.027
599
c FML008 Familial Retinoblastoma 46 0.027
600
SPC010 Speech and Communication Disorders 46 0.027
601
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.027
602
PRS063 Paresthesia 46 0.027
603
RBF001 Riboflavin Deficiency 46 0.027
604
ATX019 Ataxia with Vitamin E Deficiency 46 0.027
605
CMP034 Complete Androgen Insensitivity Syndrome 46 0.027
606
DYS015 Dysentery 45 0.027
607
c SPN311 Spinocerebellar Ataxia 13 45 0.027
608
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.027
609
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.027
610
PNM013 Pneumococcal Meningitis 45 0.027
611
DWR001 Dwarfism 45 0.027
612
c PRM038 Primary Agammaglobulinemia 45 0.027
613
c SPR009 Sporadic Breast Cancer 45 0.027
614
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 45 0.027
615
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 45 0.027
616
P ATM019 Autoimmune Polyendocrine Syndrome 45 0.027
617
SPC005 Speech Disorder 44 0.027
618
c HYP272 Hypercholesterolemia, Familial, 3 44 0.027
619
ANX004 Anoxia 44 0.027
620
CRT015 Carotid Artery Occlusion 44 0.027
621
EHR002 Ehrlichiosis 44 0.027
622
P BLP003 Blepharospasm 43 0.027
623
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 43 0.027
624
c GM2006 Gm2 Gangliosidosis 43 0.027
625
c MLG079 Malignant Pleural Mesothelioma 43 0.027
626
P HRD018 Hair Disease 43 0.027
627
PLS030 Plasminogen Deficiency, Type I 43 0.027
628
P CRB088 Cerebral Atrophy 43 0.027
629
c MCR130 Microvascular Complications of Diabetes 6 42 0.027
630
c MCR133 Microvascular Complications of Diabetes 4 42 0.027
631
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.027
632
c ATM101 Autoimmune Gastritis 42 0.027
633
P CRV039 Cervicitis 42 0.027
634
GST020 Gastric Antral Vascular Ectasia 42 0.027
635
AMN002 Amino Acid Metabolic Disorder 42 0.027
636
RDN001 Reading Disorder 42 0.027
637
BP1002 Bap1 Tumor Predisposition Syndrome 41 0.027
638
STP004 Staphylococcal Toxic Shock Syndrome 41 0.027
639
LRG014 Large Cell Neuroendocrine Carcinoma 41 0.027
640
MRP001 Morphine Dependence 41 0.027
641
CHR008 Choroiditis 41 0.027
642
CLN044 Colon Adenoma 41 0.027
643
HRD005 Hard Palate Cancer 41 0.027
644
ALL014 Allergic Encephalomyelitis 40 0.027
645
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.027
646
MLT028 Multiminicore Disease 40 0.027
647
ART008 Arteriosclerosis Obliterans 40 0.027
648
c ATM002 Autoimmune Polyendocrine Syndrome Type 1 40 0.027
649
NRD001 Neurodermatitis 40 0.027
650
c PRS097 Prostate Cancer, Hereditary, 1 40 0.027
651
WLL004 Wallerian Degeneration 40 0.027
652
HMR023 Hemorrhagic Cystitis 40 0.027
653
PLT015 Platelet Aggregation, Spontaneous 40 0.027
654
c OVR114 Ovarian Cancer 1 39 0.027
655
GST012 Gastroesophageal Junction Adenocarcinoma 39 0.027
656
C1N001 C1 Inhibitor Deficiency 39 0.027
657
OVR094 Ovarian Epithelial Cancer 39 0.027
658
HNZ004 Heinz Body Anemias 39 0.027
659
CHL147 Chlamydia Pneumonia 39 0.027
660
ZKV001 Zika Virus Infection 39 0.027
661
ATX010 Ataxia Neuropathy Spectrum 39 0.027
662
c MCP045 Mucopolysaccharidosis, Type Iiic 39 0.027
663
BTN004 Biotin Deficiency 38 0.027
664
STR077 Streptococcal Toxic-Shock Syndrome 38 0.027
665
NDL024 Nodal Marginal Zone Lymphoma 37 0.027
666
CNS002 Constrictive Pericarditis 37 0.027
667
MYL074 Myelodysplastic Syndrome with Excess Blasts 37 0.027
668
GNT033 Genetic Prion Diseases 37 0.027
669
HPT008 Hepatic Tuberculosis 37 0.027
670
c MCP048 Mucopolysaccharidosis, Type Ivb 37 0.027
671
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.027
672
c INC015 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 2 37 0.027
673
MTG002 Mutagen Sensitivity 37 0.027
674
CHR178 Chromosomal Triplication 36 0.027
675
c PRG020 Paragangliomas 3 36 0.027
676
P AXN001 Axonal Neuropathy 36 0.027
677
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.027
678
c HYP581 Hypotrichosis 6 36 0.027
679
CNT057 Central Centrifugal Cicatricial Alopecia 36 0.027
680
c CHR682 Chronic Bilirubin Encephalopathy 36 0.027
681
BRN018 Borna Disease 36 0.027
682
c RTN066 Retinitis Pigmentosa 4 35 0.027
683
END011 Endometriosis of Ovary 35 0.027
684
CHL050 Cholesterol Ester Storage Disease 35 0.027
686
DXR001 Doxorubicin Induced Cardiomyopathy 34 0.027
687
EXT054 Extra-Adrenal Pheochromocytoma 34 0.027
688
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.027
689
CND006 Candida Glabrata 33 0.027
690
HND015 Hand Skill, Relative 33 0.027
691
MLT035 Multifocal Choroiditis 33 0.027
692
c INC031 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 3 32 0.027
693
RFR009 Refractory Cytopenia with Multilineage Dysplasia 32 0.027
694
c FBR070 Febrile Seizures, Familial, 8 31 0.027
695
THY069 Thyroid Hormone Resistance, Selective Pituitary 30 0.027
696
c STR040 Stargardt Disease 3 29 0.027
697
SPL005 Splenic Artery Aneurysm 29 0.027
698
c RNG008 Ring Chromosome 13 29 0.027
699
HRD084 Hereditary Cerebral Amyloid Angiopathy 29 0.027
700
HYP346 Hypotrichosis and Recurrent Skin Vesicles 29 0.027
701
LVR014 Liver Sarcoma 29 0.027
702
P ACT232 Acute Necrotizing Encephalopathy 28 0.027
703
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.027
704
CRL001 Cerulean Cataract 27 0.027
705
HMC001 Homocarnosinosis 27 0.027
706
STN013 Stenotrophomonas Maltophilia Infection 26 0.027
707
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.027
708
P CLL020 Collagenopathy Type 2 Alpha 1 25 0.027
709
CRN042 Carnosinemia 25 0.027
710
BRN053 Bronchial Adenomas/carcinoids Childhood 25 0.027
711
HMN001 Human Monocytic Ehrlichiosis 25 0.027
712
EPD052 Epidermolysis Bullosa Simplex Superficialis 24 0.027
713
MCT002 Mct8-Specific Thyroid Hormone Cell-Membrane Transporter Deficiency 22 0.027
714
STP007 Staphylococcal Scarlet Fever 22 0.027
715
OBS097 Obsolete: Heinz Body Anemia 22 0.027
716
EXT062 Extracranial Carotid Artery Aneurysm 21 0.027
717
CNG171 Congenital Plasminogen Deficiency 19 0.027
718
c HRD156 Hereditary Central Diabetes Insipidus 19 0.027
719
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 19 0.027
720
CRD009 Cardioencephalomyopathy 19 0.027
721
BLN008 Blind Hypotensive Eye 18 0.027
722
THY116 Thyroid Carcinoma, Nonmedullary, with or Without Cell Oxyphilia 18 0.027
723
BLD137 Blood Group--Ahonen 17 0.027
724
IMM165 Immunoglobulin Switch Sequences 16 0.027
725
CHR254 Chromosome 5q Duplication 14 0.027
726
DMN042 Diaminopentanuria 13 0.027
Content
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