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Search results for grn

398 hits were found for grn

# Family MCID Name MIFTS Score
2
FRN006 Frontotemporal Dementia 68 79.584
4
c CRD166 Ceroid Lipofuscinosis, Neuronal, 11 44 55.269
5
c ADL066 Adult Neuronal Ceroid Lipofuscinosis 46 47.960
6
PRG033 Progressive Non-Fluent Aphasia 52 45.830
7
P DMN002 Dementia 66 32.642
8
GRN059 Grn Frontotemporal Dementia 16 32.198
9
APH002 Aphasia 56 25.834
10
P ALZ034 Alzheimer Disease 87 25.587
11
SMN008 Semantic Dementia 47 21.044
12
c AMY091 Amyotrophic Lateral Sclerosis 1 88 20.307
13
P NRN021 Neuronal Ceroid Lipofuscinosis 65 19.816
14
P BRS047 Breast Cancer 98 19.273
15
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 63 17.733
16
P MTR014 Motor Neuron Disease 65 17.435
17
PCK003 Pick Disease of Brain 69 16.460
18
P OVR042 Ovarian Cancer 88 15.322
19
APR001 Apraxia 52 15.287
20
P DYS154 Dystonia 64 12.494
21
SPC010 Speech and Communication Disorders 48 11.584
22
ADR005 Adrenal Carcinoma 62 11.500
23
P SPR120 Supranuclear Palsy, Progressive, 1 69 11.109
24
P TRT010 Teratoma 51 10.993
25
c PRM108 Primary Progressive Multiple Sclerosis 51 10.578
26
OBS002 Obsessive-Compulsive Disorder 68 10.409
27
PRR007 Perry Syndrome 52 10.273
28
P SZR006 Seizure Disorder 70 9.697
29
NRN005 Neuronal Ceroid-Lipofuscinoses 61 9.692
30
P MVM001 Movement Disease 61 9.426
31
P LTR001 Lateral Sclerosis 58 9.314
32
CRT033 Corticobasal Degeneration 47 9.271
33
P CNR004 Cone-Rod Dystrophy 2 74 8.976
34
IMP006 Impulse Control Disorder 45 8.976
35
DMN031 Dementia, Lewy Body 65 8.890
36
VSL003 Visual Agnosia 33 8.840
37
DYS003 Dysgraphia 35 8.840
38
DYS004 Dyscalculia 35 8.612
39
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 8.438
40
MTS001 Mutism 44 8.410
41
P PRK039 Parkinsonism 55 7.985
42
GTP001 Gait Apraxia 29 7.895
43
NMN001 Nominal Aphasia 40 7.805
44
FSC002 Fascioliasis 44 7.225
45
c FRN059 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 7 47 6.928
46
AMS001 Amusia 24 6.928
47
ASS001 Associative Agnosia 24 6.928
48
WRT002 Writing Disorder 25 6.928
49
AGR018 Agraphia 37 6.928
50
GRS001 Gerstmann Syndrome 41 6.928
51
P PRS013 Prosopagnosia 36 6.928
52
SPC005 Speech Disorder 45 6.928
53
ECH002 Echolalia 33 6.928
54
ALX001 Alexia 44 6.928
55
IDM001 Ideomotor Apraxia 37 6.928
56
P PLY180 Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy 1 56 6.854
57
CLR009 Color Agnosia 26 6.347
58
APP006 Apperceptive Agnosia 18 6.347
59
SPC003 Specific Developmental Disorder 29 6.347
60
PRP015 Paraphilia Disorder 31 6.347
61
c MNT179 Mental Retardation, Autosomal Dominant 21 36 6.347
62
c SPN201 Spinocerebellar Ataxia, Autosomal Recessive 7 45 6.347
63
c CRD182 Ceroid Lipofuscinosis, Neuronal, 10 51 6.347
64
DSS008 Disease of Mental Health 74 6.347
65
KLV001 Kluver-Bucy Syndrome 34 6.347
66
BSP005 Basophilic Adenocarcinoma 14 6.347
67
PDP001 Pedophilia 29 6.347
68
CLN003 Clonorchiasis 43 6.347
69
MLD018 Mild Cognitive Impairment 48 4.975
70
AGN016 Aging 54 4.805
71
P HPT023 Hepatocellular Carcinoma 96 4.638
72
CHL065 Cholangiocarcinoma 58 3.994
73
INT079 Intrahepatic Cholangiocarcinoma 51 3.994
74
LYS002 Lysosomal Storage Disease 51 3.626
75
PST086 Posterior Cortical Atrophy 36 3.492
76
P MYC033 Myoclonus 47 3.279
77
MLT157 Multiple System Atrophy 1 69 3.214
78
P AGN002 Agnosia 54 3.210
79
SQM006 Squamous Cell Carcinoma 60 3.158
80
CRT072 Creutzfeldt-Jakob Disease 68 3.148
81
STR067 Stroke, Ischemic 80 2.970
82
P CRB088 Cerebral Atrophy 33 2.963
83
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 2.911
84
P BPL003 Bipolar Disorder 56 2.903
85
P BCL017 B-Cell Lymphoma 59 2.633
86
DYS073 Dysphagia 53 2.567
87
P NRB001 Neuroblastoma 66 2.534
88
P PRK057 Parkinson Disease, Late-Onset 80 2.502
89
P LKM071 Leukemia, Chronic Lymphocytic 75 2.483
90
GLB002 Glioblastoma 67 2.426
91
SPC030 Specific Language Disorder 25 2.385
92
TRM010 Traumatic Brain Injury 51 2.377
93
C9R003 C9orf72 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 11 2.377
94
BRN071 Brain Injury 50 2.377
95
P PRS038 Personality Disorder 65 2.370
96
c MJR022 Major Affective Disorder 8 38 2.322
97
c MJR024 Major Affective Disorder 9 41 2.322
98
P GST053 Gastric Cancer 83 2.273
99
ETN001 Eating Disorder 59 2.273
100
P LNG032 Lung Cancer 98 2.272
101
CRB039 Cerebrovascular Disease 66 2.265
102
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 36 2.150
103
P PRS040 Prostate Cancer 95 2.150
104
HLX001 Helix Syndrome 48 2.150
105
ORL015 Oral Squamous Cell Carcinoma 43 2.090
106
P MLT020 Multiple Sclerosis 79 2.027
107
MNT002 Mental Depression 57 2.014
108
DPR016 Depression 65 2.014
109
LGP003 Logopenic Progressive Aphasia 23 2.014
110
OPS001 Opisthorchiasis 41 1.963
111
P MJR001 Major Depressive Disorder 68 1.922
112
P RTN008 Retinitis Pigmentosa 80 1.912
113
NRR001 Neuroretinitis 42 1.912
114
RTN023 Retinitis 46 1.912
115
LNG039 Lung Squamous Cell Carcinoma 57 1.912
116
P END044 Endometriosis 62 1.912
117
c SML038 Small Cell Cancer of the Lung 69 1.901
118
P SCH015 Schizophrenia 74 1.896
119
P RTN016 Retinal Degeneration 52 1.827
120
P LKM002 Leukemia 67 1.827
121
ATM095 Autoimmune Disease 61 1.822
122
P MLN008 Melanoma 76 1.806
123
P CLR023 Colorectal Cancer 100 1.756
124
P INF037 Inflammatory Bowel Disease 53 1.756
125
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.756
126
ENT011 Enterocolitis 55 1.756
127
HYP056 Hypoglycemia 65 1.756
128
PRN019 Perinatal Necrotizing Enterocolitis 60 1.756
129
VSC002 Vascular Dementia 60 1.714
130
OCL015 Oculomotor Apraxia 39 1.684
131
c SPN225 Spondyloarthropathy 1 70 1.684
132
SML010 Simultanagnosia 32 1.684
133
SPN051 Spondylitis 51 1.684
134
INF009 Inflammatory Spondylopathy 30 1.684
135
ART140 Arteries, Anomalies of 53 1.681
136
c SYS001 Systemic Lupus Erythematosus 87 1.681
137
LPP008 Lipoprotein Quantitative Trait Locus 65 1.681
138
P LPS004 Lupus Erythematosus 61 1.681
139
TRN018 Transitional Cell Carcinoma 56 1.681
140
KHL003 Kohlschutter-Tonz Syndrome 59 1.679
141
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 67 1.679
142
ANX004 Anoxia 40 1.603
143
RPD005 Rapidly Involuting Congenital Hemangioma 46 1.603
144
47X002 47,xyy 48 1.603
145
P AMY004 Amyloidosis 70 1.594
146
MCR011 Microinvasive Gastric Cancer 41 1.548
147
P RSP003 Respiratory Failure 74 1.548
148
P BLD134 Bladder Cancer 79 1.520
149
P FRG001 Fragile X Syndrome 70 1.520
150
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.520
151
P CHL066 Cholangitis 52 1.520
152
CHL067 Cholecystitis 60 1.520
153
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 1.494
154
P TRM003 Tremor 48 1.459
155
MDD011 Mood Disorder 62 1.459
156
c ART115 Aortic Valve Disease 1 74 1.433
157
c SCN036 Secondary Progressive Multiple Sclerosis 55 1.433
158
PRM329 Premature Aging 36 1.433
159
SVR001 Severe Acute Respiratory Syndrome 67 1.433
160
CNS004 Constipation 56 1.433
161
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.433
162
ISC004 Ischemia 61 1.433
163
DMY004 Demyelinating Disease 50 1.433
164
P MTC069 Mitochondrial Disorders 57 1.433
165
PRT036 Peritonitis 65 1.395
166
FLL027 Fallopian Tube Carcinoma 67 1.395
167
P HYP263 Hypersomnia 41 1.387
168
ATH013 Atherosclerosis Susceptibility 63 1.341
169
P OST002 Osteoporosis 76 1.341
170
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.341
171
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.341
172
c LKM061 Leukemia, Acute Myeloid 83 1.341
173
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 1.341
174
P GCH001 Gaucher's Disease 70 1.341
175
P HRT032 Heart Disease 81 1.341
176
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.298
177
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 1.298
178
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.298
179
P PRN023 Prion Disease 60 1.298
180
CHR073 Choreatic Disease 54 1.298
181
P RHM011 Rheumatoid Arthritis 82 1.241
182
GRN034 Grange Syndrome 36 1.241
183
c PCH010 Pachyonychia Congenita 3 43 1.241
184
c BCT013 Bacterial Pneumonia 48 1.241
185
P LNG064 Lung Cancer Susceptibility 3 70 1.241
186
P ADN016 Adenocarcinoma 63 1.241
187
BRN024 Bronchitis 67 1.241
188
GST023 Gastric Ulcer 52 1.241
189
HMP009 Haemophilus Influenzae 41 1.241
190
PRP016 Paraplegia 52 1.177
191
CKT002 Cakut 47 1.133
192
CVD001 Covid-19 57 1.133
193
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 1.133
194
GRN045 Granulosis Rubra Nasi 15 1.133
195
INT323 Intraocular Pressure Quantitative Trait Locus 64 1.133
196
P HRS035 Hirschsprung Disease 1 66 1.133
197
HRW001 Hair Whorl 35 1.133
198
P MYP004 Myopathy 67 1.133
199
GLL048 Glial Tumor 52 1.133
200
HYP066 Hyperglycemia 61 1.133
201
P GST044 Gastritis 55 1.133
202
CMM005 Common Cold 56 1.133
203
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.133
204
GLM045 Glioma 63 1.133
205
P ENC018 Encephalopathy 62 1.088
206
P LKM062 Leukemia, Acute Lymphoblastic 69 1.024
207
PLY100 Polyploidy 36 1.014
208
PPL052 Papillomatosis, Confluent and Reticulated 34 1.014
209
MLR004 Malaria 80 1.014
210
DFF005 Diffuse Large B-Cell Lymphoma 54 1.014
211
KPS004 Kaposi Sarcoma 77 1.014
212
P RTN024 Retinoblastoma 73 1.014
213
P INF038 Influenza 68 1.014
214
MLT177 Multisystem Proteinopathy 31 1.014
215
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.014
216
CHM008 Chmp2b Frontotemporal Dementia 12 1.014
217
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 1.006
218
P ATS364 Autism 69 0.878
219
PFF001 Pfeiffer Syndrome 77 0.878
220
c SPS151 Spastic Paraplegia 11, Autosomal Recessive 49 0.878
221
PLY150 Polykaryocytosis Inducer 29 0.878
222
c MST023 Mesothelioma, Malignant 56 0.878
223
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.878
224
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.878
225
P HNT016 Huntington Disease 73 0.878
226
P BLD062 Bile Duct Cancer 67 0.878
227
BLD131 Bladder Urothelial Carcinoma 60 0.878
228
P MNC007 Monocytic Leukemia 47 0.878
229
c BPL002 Bipolar I Disorder 47 0.878
230
P HYP086 Hypothyroidism 69 0.878
231
TTN003 Tetanus 65 0.878
232
CNG034 Congestive Heart Failure 69 0.878
233
P PGT001 Paget's Disease of Bone 61 0.878
234
P BNG032 Benign Mesothelioma 53 0.878
235
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.878
236
ALL014 Allergic Encephalomyelitis 34 0.878
237
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.821
238
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.821
239
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.821
240
CHR158 Charles Bonnet Syndrome 23 0.821
241
DWN001 Down Syndrome 70 0.722
242
LNG031 Lung Benign Neoplasm 51 0.722
243
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 0.717
244
SPN186 Spinal Cord Injury 61 0.717
245
BNG077 Benign Idiopathic Neonatal Seizures 23 0.717
246
ALL003 Allergic Rhinitis 67 0.717
247
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 55 0.717
248
c AMY113 Amyotrophic Lateral Sclerosis 12 with or Without Frontotemporal Dementia 28 0.717
249
c SPN309 Spinocerebellar Ataxia 6 58 0.717
250
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.717
251
c FRN045 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 4 36 0.717
252
EWN003 Ewing Sarcoma 70 0.717
253
EPL199 Epilepsy, Progressive Myoclonic, 4, with or Without Renal Failure 36 0.717
254
c TRC092 Trichorhinophalangeal Syndrome, Type I 54 0.717
255
c RTN150 Retinitis Pigmentosa 10 44 0.717
256
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.717
257
THY029 Thyroid Carcinoma 51 0.717
258
PRT037 Pertussis 65 0.717
259
P MSC003 Muscular Atrophy 52 0.717
260
P MYL006 Myeloid Leukemia 61 0.717
261
PST092 Posttransplant Acute Limbic Encephalitis 28 0.717
262
P RRN010 Rare Neurodegenerative Disease 14 0.717
263
LYM009 Lymphocytic Choriomeningitis 46 0.717
264
P SPN046 Spinal Muscular Atrophy 63 0.717
265
SNS003 Sensory Peripheral Neuropathy 52 0.717
266
MCR013 Microphthalmia 60 0.717
267
P RHN004 Rhinitis 57 0.717
268
THR012 Thoracic Cancer 44 0.717
269
P MLT074 Multiple Endocrine Neoplasia 59 0.717
270
CYT002 Cytokine Deficiency 43 0.717
271
MD2001 Med23 20 0.717
272
OVR094 Ovarian Epithelial Cancer 39 0.717
273
P BLD124 Bleeding Disorder, Platelet-Type, 11 67 0.673
274
SKN019 Skin Melanoma 71 0.673
275
CRB211 Cerebral Cortical Dysplasia 21 0.581
276
HNM002 Hinman Syndrome 27 0.581
277
DFN245 Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct 50 0.581
278
KR002 Kuru 45 0.581
279
CGN007 Cognitive Function 1, Social 27 0.581
280
ART002 Arts Syndrome 66 0.581
281
P DYS193 Dystonia 11, Myoclonic 55 0.581
282
GRS011 Gerstmann-Straussler Disease 56 0.581
283
PPL049 Papillon-Lefevre Syndrome 66 0.581
284
ADT001 Auditory Agnosia 26 0.581
285
c SPN444 Spinal Muscular Atrophy Type 0 22 0.581
286
P FTL002 Fatal Familial Insomnia 50 0.581
287
c FNC043 Fanconi Anemia, Complementation Group E 62 0.581
288
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.581
289
c SPL067 Split-Hand/foot Malformation 1 46 0.581
290
c BRN108 Branchiootic Syndrome 1 62 0.581
291
NRN008 Neuronal Intranuclear Inclusion Disease 47 0.581
292
P ATR001 Atrioventricular Septal Defect 55 0.581
293
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 54 0.581
294
GLS018 Glass Syndrome 61 0.581
295
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 0.581
296
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 0.581
297
PNM010 Pneumothorax, Primary Spontaneous 58 0.581
298
HND015 Hand Skill, Relative 30 0.581
299
ADP007 Adie Pupil 40 0.581
300
ADL002 Adult Syndrome 70 0.581
302
APR010 Apraxia of Eyelid Opening 15 0.581
303
AKN002 Akinetic Mutism 36 0.581
304
SCR011 Scrapie 39 0.581
305
RMS001 Rem Sleep Behavior Disorder 47 0.581
306
LRN003 Learning Disability 49 0.581
307
PRM153 Primary Progressive Apraxia of Speech 13 0.581
308
CNV002 Conversion Disorder 47 0.581
309
P EPL164 Epilepsy 68 0.581
310
P OLV001 Olivopontocerebellar Atrophy 51 0.581
311
FBR047 Fibromyalgia 58 0.581
312
ERD001 Erdheim-Chester Disease 53 0.581
313
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.581
314
ASY002 Asymptomatic Neurosyphilis 41 0.581
315
CNJ001 Conjugate Gaze Palsy 30 0.581
316
PTH002 Pathological Gambling 48 0.581
317
P DYS005 Dyslexia 41 0.581
318
RDN001 Reading Disorder 40 0.581
319
AMN003 Amnestic Disorder 54 0.581
320
MYS004 Myiasis 39 0.581
321
IRN002 Iron Metabolism Disease 57 0.581
322
TRN012 Transient Global Amnesia 38 0.581
323
FXC001 Foix Chavany Marie Syndrome 27 0.581
324
NRS003 Neurosyphilis 45 0.581
325
P PNC035 Pancreatic Cancer 86 0.517
326
P GLM040 Glioma Susceptibility 1 71 0.517
327
c INH030 Inherited Retinal Disorder 28 0.507
328
c RRP028 Rare Epilepsy 17 0.507
329
SPS057 Spasticity 42 0.507
330
P MCH002 Machado-Joseph Disease 62 0.507
331
RTN187 Retinitis Pigmentosa-Deafness Syndrome 48 0.507
332
ANX010 Anxiety 70 0.507
333
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.507
334
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.507
335
GST092 Gastroesophageal Reflux 61 0.507
336
WLL001 Williams-Beuren Syndrome 61 0.507
337
OCL008 Oculopharyngeal Muscular Dystrophy 53 0.507
338
P ATX030 Ataxia-Telangiectasia 80 0.507
339
MNT001 Mantle Cell Lymphoma 67 0.507
340
c IGN002 Iga Nephropathy 2 19 0.507
341
c FRN060 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 6 27 0.507
342
PRT251 Proteinuria, Chronic Benign 57 0.507
343
c ATS007 Autism Spectrum Disorder 72 0.507
344
BNR002 Bone Resorption Disease 47 0.507
345
c AMY023 Amyotrophic Lateral Sclerosis Type 6 34 0.507
346
P USH001 Usher Syndrome 64 0.507
347
P CHN012 Chondrosarcoma 57 0.507
348
P SPN301 Spinocerebellar Ataxia 2 59 0.507
349
c PRK071 Parkinson Disease 14, Autosomal Recessive 42 0.507
350
c IGN004 Iga Nephropathy 3 22 0.507
351
TBL029 Tubulin, Beta 28 0.507
352
c AMY105 Amyotrophic Lateral Sclerosis 6 with or Without Frontotemporal Dementia 33 0.507
353
CLB019 Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly 43 0.507
354
CRD075 Ceroid Lipofuscinosis, Neuronal, 8, Northern Epilepsy Variant 46 0.507
355
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 0.507
356
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 50 0.507
357
OVR105 Ovarian Serous Carcinoma 37 0.507
358
P LKD001 Leukodystrophy 59 0.507
359
GLC003 Glucose Intolerance 54 0.507
361
c ACT073 Acute Leukemia 58 0.507
362
AVN001 Avian Influenza 61 0.507
363
ART010 Arteriolosclerosis 37 0.507
364
FND002 Fundus Dystrophy 55 0.507
365
P MSC005 Muscular Dystrophy 67 0.507
366
MTR086 Motor Stereotypies 14 0.507
367
IGG001 Iga Glomerulonephritis 50 0.507
368
ADN018 Adenoma 59 0.507
369
OST012 Osteoarthritis 77 0.507
370
c SPS126 Spastic Paraplegia 49, Autosomal Recessive 44 0.507
371
c HYP532 Hypogonadotropic Hypogonadism 18 with or Without Anosmia 27 0.507
372
P SNS001 Sensorineural Hearing Loss 59 0.507
373
CRB004 Cerebral Artery Occlusion 45 0.507
374
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.507
375
PLV003 Pelvic Inflammatory Disease 55 0.507
376
TLN003 Telangiectasis 51 0.507
377
NRX001 Neuroaxonal Dystrophy 38 0.507
378
CLB002 Clubfoot 51 0.507
379
P HPT021 Hepatitis 69 0.507
380
SCH014 Schistosomiasis 56 0.507
381
SRC014 Sarcoma 65 0.507
382
MST005 Mastitis 53 0.507
383
P SLP005 Sleep Disorder 61 0.507
384
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.507
385
P RTN018 Retinal Disease 53 0.507
386
EPL001 Epilepsy with Generalized Tonic-Clonic Seizures 40 0.507
387
P KDN017 Kidney Cancer 61 0.507
388
P LPS002 Liposarcoma 64 0.507
389
MMM001 Mammary Paget's Disease 53 0.507
390
c HPT016 Hepatitis B 62 0.507
391
LRR002 Lrrk2 Parkinson Disease 9 0.507
392
P TRC031 Trichorhinophalangeal Syndrome 38 0.507
393
ORL011 Oral Cancer 60 0.507
394
c SPS230 Spastic Paraplegia Type 49 10 0.507
395
48X005 48,xyyy 39 0.507
396
CLN039 Cln4 Disease 17 0.507
397
P DYS021 Dysautonomia 38 0.507
398
PSD088 Pseudobulbar Affect 33 0.507
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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