Search results for ca2

373 hits were found for ca2

# Family MCID Name MIFTS Score
1
c OST163 Osteopetrosis, Autosomal Recessive 3 33 5.232
2
P OST001 Osteopetrosis 70 4.719
3
P PNC035 Pancreatic Cancer 89 4.409
4
P RNL007 Renal Tubular Acidosis 51 4.371
5
P OST002 Osteoporosis 75 3.557
6
P CHL066 Cholangitis 52 3.557
7
MTB004 Metabolic Acidosis 49 3.557
8
BRD001 Brody Myopathy 41 3.179
9
P PRM006 Primary Biliary Cirrhosis 55 3.081
10
PSD007 Pseudomyxoma Peritonei 54 3.081
11
OCL006 Ocular Hypertension 51 3.081
12
MYX001 Myxopapillary Ependymoma 44 3.081
13
c ATM024 Autoimmune Pancreatitis 49 2.515
14
FBL008 Fibular Aplasia or Hypoplasia, Femoral Bowing and Poly-, Syn-, and Oligodactyly 48 2.515
15
NRR001 Neuroretinitis 46 2.515
16
ARR018 Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 42 2.515
17
P RNL045 Renal Tubular Acidosis, Distal 42 2.515
18
P RPP006 Rippling Muscle Disease 2 42 2.515
19
RTN013 Retinal Hemangioblastoma 38 2.515
20
CHR667 Chromosome 3pter-P25 Deletion Syndrome 37 2.515
21
CLR012 Clear Cell Adenofibroma 35 2.515
22
ACT056 Acute Cor Pulmonale 34 2.515
23
c RTN134 Retinitis Pigmentosa 40 32 2.515
24
ATM076 Autoimmune Retinopathy 30 2.515
25
NRG001 Neurogenic Bowel 29 2.515
26
MLS013 Miles-Carpenter Syndrome 28 2.515
27
DNT046 Dental Abscess 28 2.515
28
P ACT080 Acute Pulmonary Heart Disease 24 2.515
29
c BLD140 Blood Group, I System 37 0.588
30
NRN002 Neuronitis 43 0.582
31
END072 Endotheliitis 46 0.452
32
P PNC044 Pancreatitis 64 0.360
33
P NRB001 Neuroblastoma 73 0.247
34
RTN023 Retinitis 52 0.205
35
c CTR122 Cataract 5, Multiple Types 38 0.205
36
PRS047 Prostatitis 59 0.195
37
P ALZ034 Alzheimer Disease 95 0.191
38
P MLG056 Malignant Hyperthermia 60 0.187
39
HYP266 Hypoxia 61 0.184
40
P PRS040 Prostate Cancer 88 0.180
41
ISC004 Ischemia 66 0.176
42
CRB009 Cerebritis 41 0.172
43
P BRS047 Breast Cancer 100 0.168
44
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.164
45
PRT037 Pertussis 70 0.156
46
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.156
47
P LKM002 Leukemia 75 0.152
48
CYS001 Cystic Fibrosis 85 0.147
49
P GLM045 Glioma 61 0.138
50
P THY032 Thyroiditis 56 0.138
51
P ATR011 Atrial Fibrillation 68 0.133
52
ANX004 Anoxia 49 0.133
53
P LNG032 Lung Cancer 99 0.127
54
INS001 Insulinoma 66 0.122
55
P HYP061 Hypertrophic Cardiomyopathy 65 0.122
56
MNT310 Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type 32 0.122
57
P AST007 Astrocytoma 66 0.110
58
c CRN243 Carney Complex, Type 1 35 0.110
59
P RNG031 Ring Chromosome Y Syndrome 29 0.110
60
c HYP595 Hypertension, Essential 78 0.104
61
AGN016 Aging 65 0.104
62
CNT105 Central Core Disease of Muscle 57 0.104
63
MYC005 Myocardial Stunning 47 0.104
64
GLB002 Glioblastoma 74 0.097
65
MLN008 Melanoma 72 0.097
66
P LYM118 Lymphoma 71 0.097
67
P ADN016 Adenocarcinoma 71 0.097
68
P KDN018 Kidney Disease 69 0.097
69
ACR006 Aceruloplasminemia 65 0.097
70
ADN018 Adenoma 63 0.097
71
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 61 0.097
72
LMB002 Lambert-Eaton Myasthenic Syndrome 58 0.097
73
MGR028 Migraine with or Without Aura 1 55 0.097
74
c FML023 Familial Hemiplegic Migraine 51 0.097
75
P HMP006 Hemiplegic Migraine 49 0.097
76
P ATX024 Ataxia-Oculomotor Apraxia 3 47 0.097
77
MNG003 Mungan Syndrome 34 0.097
78
P CLR023 Colorectal Cancer 98 0.090
79
P EPL164 Epilepsy 70 0.090
80
P MYP004 Myopathy 69 0.090
81
c SML038 Small Cell Cancer of the Lung 67 0.090
82
GNG013 Gingivitis 64 0.090
83
P RST002 Restrictive Cardiomyopathy 51 0.090
84
SCT005 Scott Syndrome 48 0.090
85
PHC013 Phaeochromocytoma 44 0.090
86
MLG086 Malignant Hyperthermia Susceptibility 38 0.090
87
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.090
88
AST005 Asthma 83 0.082
89
P ART022 Arthritis 77 0.082
90
P DLT002 Dilated Cardiomyopathy 76 0.082
91
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.082
92
P PLY014 Polycystic Kidney Disease 60 0.082
93
ORL011 Oral Cancer 60 0.082
94
P EPS003 Episodic Ataxia 57 0.082
95
P PTT006 Pituitary Adenoma 57 0.082
96
P HYP726 Hypercalcemia, Infantile, 1 57 0.082
97
P RNL015 Renal Hypertension 46 0.082
98
c PCH010 Pachyonychia Congenita 3 38 0.082
99
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.082
100
P HPT023 Hepatocellular Carcinoma 94 0.074
101
P RHM011 Rheumatoid Arthritis 91 0.074
102
P MYC007 Myocardial Infarction 81 0.074
103
CRH001 Crohn's Disease 80 0.074
104
P DBT009 Diabetes Mellitus 72 0.074
105
DMN002 Dementia 68 0.074
106
P ESP024 Esophagitis 64 0.074
107
P NRP001 Neuropathy 63 0.074
108
THR024 Thrombosis 61 0.074
109
P INF037 Inflammatory Bowel Disease 52 0.074
110
P ATS308 Autosomal Dominant Cerebellar Ataxia 47 0.074
111
c BRN108 Branchiootic Syndrome 1 47 0.074
112
BRN080 Brain Ischemia 45 0.074
113
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.074
114
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.064
115
P AMY004 Amyloidosis 69 0.064
116
P MYL006 Myeloid Leukemia 69 0.064
117
c MYT021 Myotonic Dystrophy 1 68 0.064
118
P PRD008 Periodontitis 67 0.064
119
P INT068 Intestinal Disease 65 0.064
120
P WLF004 Wolfram Syndrome 61 0.064
121
P BPL003 Bipolar Disorder 61 0.064
122
P INF032 Infertility 59 0.064
123
P HYP069 Hyperparathyroidism 58 0.064
124
P LTR001 Lateral Sclerosis 58 0.064
125
CHL014 Cholera 56 0.064
126
HPT022 Hepatoblastoma 55 0.064
127
c EPS035 Episodic Ataxia, Type 2 54 0.064
128
TMT001 Timothy Syndrome 52 0.064
129
P NGH001 Night Blindness 51 0.064
130
P MYT002 Myotonic Dystrophy 50 0.064
131
PTT037 Pituitary Tumors 49 0.064
132
P FML068 Familial Hypocalciuric Hypercalcemia 49 0.064
133
c SPN309 Spinocerebellar Ataxia 6 48 0.064
134
CRN017 Coronary Thrombosis 48 0.064
135
c MGR032 Migraine, Familial Hemiplegic, 1 32 0.064
136
P OVR042 Ovarian Cancer 82 0.052
137
P HRT032 Heart Disease 80 0.052
138
P PLM037 Pulmonary Hypertension 79 0.052
139
P HPT021 Hepatitis 75 0.052
140
SQM006 Squamous Cell Carcinoma 74 0.052
141
CNG034 Congestive Heart Failure 74 0.052
142
P CRV035 Cervical Cancer 72 0.052
143
c CHR089 Chronic Kidney Failure 72 0.052
144
P NSP012 Nasopharyngeal Carcinoma 71 0.052
145
CHL065 Cholangiocarcinoma 70 0.052
146
P CHR071 Charcot-Marie-Tooth Disease 67 0.052
147
P MCL013 Mucolipidosis Iv 67 0.052
148
GST050 Gastrointestinal System Disease 66 0.052
149
GST045 Gastroenteritis 65 0.052
150
P THY109 Thyroid Cancer, Nonmedullary, 1 64 0.052
151
P LNG028 Long Qt Syndrome 63 0.052
152
RFS006 Refsum Disease, Classic 63 0.052
153
P SPN046 Spinal Muscular Atrophy 63 0.052
154
CLT003 Colitis 63 0.052
155
KRT019 Keratitis, Hereditary 62 0.052
156
MCS002 Mucositis 61 0.052
157
P RHB003 Rhabdomyosarcoma 61 0.052
158
ALL006 Allergic Asthma 60 0.052
159
END030 End Stage Renal Failure 59 0.052
160
CHL067 Cholecystitis 58 0.052
161
NRN004 Neuroendocrine Tumor 58 0.052
162
VSC002 Vascular Dementia 58 0.052
163
BRN004 Brain Edema 57 0.052
164
P CYS018 Cystitis 57 0.052
165
P CNG010 Congenital Stationary Night Blindness 56 0.052
166
P MSC003 Muscular Atrophy 55 0.052
167
P ICH004 Ichthyosis 54 0.052
168
TTH006 Tooth Disease 54 0.052
169
c INF071 Inflammatory Bowel Disease 1 54 0.052
170
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.052
171
MLN007 Male Infertility 53 0.052
172
PRT038 Protein-Energy Malnutrition 52 0.052
173
CRD223 Cardiac Arrhythmia 52 0.052
174
ILT001 Ileitis 52 0.052
175
c MYP132 Myopathy, Congenital 51 0.052
176
P CRV039 Cervicitis 49 0.052
177
EPL073 Epilepsy, Nocturnal Frontal Lobe, 1 47 0.052
178
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.052
179
DST006 Diastolic Heart Failure 47 0.052
180
NSP002 Nasopharyngitis 46 0.052
181
MRP001 Morphine Dependence 43 0.052
182
TRT001 Teratocarcinoma 41 0.052
183
ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 37 0.052
184
KRT028 Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant 32 0.052
185
c CTR119 Cataract 32, Multiple Types 32 0.052
186
c NGH025 Night Blindness, Congenital Stationary, Type 2a 31 0.052
187
PLT031 Platelet Membrane Fluidity 29 0.052
188
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.037
189
c SYS001 Systemic Lupus Erythematosus 86 0.037
190
MLR004 Malaria 86 0.037
191
P MLT020 Multiple Sclerosis 85 0.037
192
GST053 Gastric Cancer 84 0.037
193
INS024 Insulin-Like Growth Factor I 83 0.037
194
P RTT002 Rett Syndrome 82 0.037
195
P RTN008 Retinitis Pigmentosa 81 0.037
196
P ATX030 Ataxia-Telangiectasia 80 0.037
197
ULC004 Ulcerative Colitis 80 0.037
198
P BLD134 Bladder Cancer 78 0.037
199
P RTN024 Retinoblastoma 76 0.037
200
END057 Endometrial Cancer 76 0.037
201
P MYL005 Myelofibrosis 75 0.037
202
c LKM071 Leukemia, Chronic Lymphocytic 75 0.037
203
MRF001 Marfan Syndrome 75 0.037
204
MSC157 Muscular Dystrophy, Duchenne Type 74 0.037
205
P PHC003 Pheochromocytoma 72 0.037
206
KWS002 Kawasaki Disease 72 0.037
207
VSC007 Vascular Disease 71 0.037
208
HMN044 Human Immunodeficiency Virus Type 1 71 0.037
209
P SCH015 Schizophrenia 71 0.037
210
ART016 Aortic Aneurysm 70 0.037
211
P ATS364 Autism 70 0.037
212
P LPS004 Lupus Erythematosus 69 0.037
213
P TBR001 Tuberous Sclerosis 69 0.037
214
P MYC084 Mycobacterium Tuberculosis 1 69 0.037
215
CNR004 Cone-Rod Dystrophy 2 69 0.037
216
P CRN018 Coronary Artery Anomaly 69 0.037
217
P PLM036 Pulmonary Fibrosis 68 0.037
218
GLB015 Glioblastoma Multiforme 68 0.037
219
P ART023 Arthropathy 68 0.037
220
P ADL010 Adult Respiratory Distress Syndrome 67 0.037
221
P CNJ013 Conjunctivitis 67 0.037
222
P MSC005 Muscular Dystrophy 66 0.037
223
ATM095 Autoimmune Disease 66 0.037
224
c MLG068 Malignant Glioma 66 0.037
225
SND001 Sandhoff Disease 65 0.037
226
P PSR002 Psoriasis 65 0.037
227
CNN005 Connective Tissue Disease 65 0.037
228
TTN003 Tetanus 65 0.037
229
P ART067 Aortic Aneurysm, Familial Thoracic 1 65 0.037
230
BLL006 Bullous Pemphigoid 64 0.037
231
HYP066 Hyperglycemia 64 0.037
232
c ACT075 Acute Myocardial Infarction 64 0.037
233
HLC007 Helicobacter Pylori Infection 64 0.037
234
ADR054 Adrenocortical Carcinoma, Hereditary 63 0.037
235
RBS001 Rabies 63 0.037
236
P INT143 Interstitial Cystitis 63 0.037
237
TNG003 Tongue Cancer 63 0.037
238
c TBR025 Tuberous Sclerosis 1 63 0.037
239
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.037
240
THY111 Thyroid Carcinoma, Familial Medullary 63 0.037
241
CRD119 Cardiac Arrest 63 0.037
242
RHM027 Rheumatic Disease 62 0.037
243
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 62 0.037
244
HYP056 Hypoglycemia 62 0.037
245
P NRN021 Neuronal Ceroid Lipofuscinosis 62 0.037
246
c ACT027 Acute Pancreatitis 61 0.037
247
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.037
248
VNW001 Von Willebrand's Disease 61 0.037
249
P GLY013 Glycogen Storage Disease 61 0.037
250
ANR040 Aneurysm 61 0.037
251
P NTR004 Neutropenia 60 0.037
252
P DRR001 Diarrhea 60 0.037
253
STT001 Status Epilepticus 60 0.037
254
CLR108 Colorectal Adenoma 60 0.037
255
JNT002 Joint Disorders 60 0.037
256
DBT010 Diabetic Neuropathy 60 0.037
257
PST028 Post-Traumatic Stress Disorder 59 0.037
258
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 59 0.037
259
P FTL001 Fetal Alcohol Syndrome 59 0.037
260
P MNC007 Monocytic Leukemia 59 0.037
261
ALL026 Allergic Hypersensitivity Disease 59 0.037
262
TRN015 Transient Cerebral Ischemia 58 0.037
263
P SML001 Small Cell Carcinoma 58 0.037
264
P BRS044 Breast Adenocarcinoma 58 0.037
265
P CRN300 Coronary Heart Disease 1 57 0.037
266
P OCL002 Oculocutaneous Albinism 57 0.037
267
IMM136 Immune System Disease 57 0.037
268
ECT006 Ectodermal Dysplasia 57 0.037
269
MSC007 Muscle Hypertrophy 57 0.037
270
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 57 0.037
271
P SCL018 Scoliosis 56 0.037
272
PLY156 Polycystic Kidney Disease 4 with or Without Hepatic Disease 56 0.037
273
P RTN016 Retinal Degeneration 56 0.037
274
P CHL002 Childhood Absence Epilepsy 56 0.037
275
CLN019 Colonic Disease 55 0.037
276
PND002 Pendred Syndrome 55 0.037
277
c LKM070 Leukemia, Acute Monocytic 55 0.037
278
P AGG001 Aggressive Periodontitis 55 0.037
279
c EPL209 Epilepsy, Idiopathic Generalized 10 55 0.037
280
P HYP750 Hypertriglyceridemia, Familial 55 0.037
281
P HYP024 Hypoparathyroidism 55 0.037
282
P HYP014 Hyperuricemia 54 0.037
283
BRN071 Brain Injury 54 0.037
284
SLV012 Salivary Gland Adenoid Cystic Carcinoma 54 0.037
285
WLF002 Wolf-Hirschhorn Syndrome 54 0.037
286
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 54 0.037
287
GTR002 Goiter 53 0.037
288
P CLL015 Collagen Disease 53 0.037
289
HYP005 Hypokalemia 53 0.037
290
MSC033 Muscle Disorders 53 0.037
291
P CRD132 Cardiac Conduction Defect 53 0.037
292
P BRT004 Bartter Disease 52 0.037
293
URM002 Uremia 52 0.037
294
LMB062 Limb Ischemia 52 0.037
295
c BNG091 Benign Chronic Pemphigus 52 0.037
296
ACH005 Achalasia 52 0.037
297
P GLM040 Glioma Susceptibility 1 51 0.037
298
ART140 Arteries, Anomalies of 51 0.037
299
DRG003 Drug Dependence 51 0.037
300
PRT029 Parathyroid Adenoma 50 0.037
301
RYS001 Reye Syndrome 50 0.037
302
HMS001 Hemosiderosis 50 0.037
303
HMC014 Homocysteinemia 49 0.037
304
IMM102 Immunodeficiency 14 49 0.037
305
P GNT008 Giant Cell Tumor 49 0.037
306
PNC119 Pancreatic Neuroendocrine Tumor 49 0.037
307
P MYP087 Myopathy, Tubular Aggregate, 1 48 0.037
308
P NNT009 Neonatal Diabetes Mellitus 48 0.037
309
HYP457 Hypertrophic Scars 48 0.037
310
c LBR014 Leber Congenital Amaurosis 4 48 0.037
311
PST011 Pustulosis of Palm and Sole 47 0.037
312
P DYS021 Dysautonomia 47 0.037
313
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 47 0.037
314
ADR004 Adrenal Cortical Adenocarcinoma 47 0.037
315
c LNG048 Long Qt Syndrome 3 46 0.037
316
P AML002 Amelogenesis Imperfecta 46 0.037
317
DDN006 Duodenitis 46 0.037
318
THR035 Thrombasthenia 46 0.037
319
MYP136 Myopathy, Centronuclear, X-Linked 46 0.037
320
ALB002 Albinism 45 0.037
321
CHR466 Chronic Thromboembolic Pulmonary Hypertension 43 0.037
322
KWS001 Kwashiorkor 43 0.037
323
IDP070 Idiopathic Scoliosis 42 0.037
324
AML001 Amelanotic Melanoma 42 0.037
325
MNN017 Mononeuropathy 42 0.037
326
RST023 Resting Heart Rate, Variation in 42 0.037
327
c PLY141 Polycystic Kidney Disease 5 42 0.037
328
OCL022 Ocular Melanoma 41 0.037
329
MYT011 Myotonia 41 0.037
330
SPP011 Suppression of Tumorigenicity 12 41 0.037
331
c HYP057 Hypervitaminosis D 40 0.037
332
ADN002 Adenoiditis 40 0.037
333
CHP002 Chops Syndrome 40 0.037
334
SCN001 Secondary Hyperparathyroidism of Renal Origin 40 0.037
335
NRX001 Neuroaxonal Dystrophy 40 0.037
336
DXR001 Doxorubicin Induced Cardiomyopathy 40 0.037
337
PST055 Postural Hypotension 40 0.037
338
ALD013 Aldosterone-Producing Adenoma 39 0.037
339
ACL001 Acalculous Cholecystitis 39 0.037
340
PLY112 Polyarteritis Nodosa, Childhood-Onset 39 0.037
341
RCT017 Rectal Disease 38 0.037
342
ENT004 Enthesopathy 38 0.037
343
P HYP733 Hypercalciuria, Absorptive, 2 37 0.037
344
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 37 0.037
345
c LKM004 Leukemia, B-Cell, Chronic 37 0.037
346
LWT001 Low Tension Glaucoma 35 0.037
347
c LKM056 Leukemia, Chronic Lymphocytic 2 35 0.037
348
OVR093 Overhydrated Hereditary Stomatocytosis 35 0.037
349
c HYP555 Hypertriglyceridemia, Transient Infantile 34 0.037
350
DFF012 Differentiating Neuroblastoma 34 0.037
351
c MJR008 Major Affective Disorder 2 33 0.037
352
c MJR007 Major Affective Disorder 1 33 0.037
353
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 33 0.037
354
c MJR023 Major Affective Disorder 7 32 0.037
355
c MJR024 Major Affective Disorder 9 31 0.037
356
c MJR022 Major Affective Disorder 8 31 0.037
357
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.037
358
P MJR004 Major Affective Disorder 4 29 0.037
359
HGH001 High Pressure Neurological Syndrome 29 0.037
360
PSD040 Pseudomyotonia 28 0.037
361
c MJR003 Major Affective Disorder 6 28 0.037
362
TXC004 Toxic Diffuse Goiter 27 0.037
363
IMM065 Immunodeficiency 10 27 0.037
364
ADG002 Audiogenic Seizures 26 0.037
365
c MJR006 Major Affective Disorder 5 25 0.037
366
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 25 0.037
367
P DST101 Distal Hereditary Motor Neuropathies 24 0.037
368
IMM143 Immunodeficiency 48 24 0.037
369
PYR012 Pyruvate Dehydrogenase E1-Beta Deficiency 23 0.037
370
PRX034 Peroxisome Disorders 20 0.037
371
CRN287 Carnitine Deficiency, Myopathic 16 0.037
372
P STM009 Stomatocytosis I 16 0.037
373
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 14 0.037
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