Search results for H2AC18

415 hits were found for H2AC18

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 98 2.354
2
P LNG032 Lung Cancer 97 2.039
3
P HPT023 Hepatocellular Carcinoma 100 1.665
4
P PRS040 Prostate Cancer 97 1.665
5
P BRS047 Breast Cancer 96 1.665
6
P OVR042 Ovarian Cancer 89 1.665
8
P HRT032 Heart Disease 75 1.665
9
XRD010 Xeroderma Pigmentosum, Variant Type 73 1.665
10
P SYS005 Systemic Scleroderma 70 1.665
11
P SKN015 Skin Carcinoma 67 1.665
12
CLF027 Cleft Palate, Isolated 64 1.665
13
P CFF008 Coffin-Siris Syndrome 1 62 1.665
14
P SLV026 Salivary Gland Carcinoma 60 1.665
15
THY122 Thyroid Gland Cancer 58 1.665
16
c SYS001 Systemic Lupus Erythematosus 86 1.442
17
RDD003 Riddle Syndrome 50 1.442
18
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 1.177
19
c AMY091 Amyotrophic Lateral Sclerosis 1 89 1.177
20
MYL069 Myeloma, Multiple 85 1.177
21
c LKM061 Leukemia, Acute Myeloid 83 1.177
22
c FNC027 Fanconi Anemia, Complementation Group a 81 1.177
23
P RTT002 Rett Syndrome 80 1.177
24
SQM013 Squamous Cell Carcinoma, Head and Neck 80 1.177
25
c LKM071 Leukemia, Chronic Lymphocytic 79 1.177
26
PFF001 Pfeiffer Syndrome 79 1.177
27
RNL114 Renal Cell Carcinoma, Nonpapillary 78 1.177
28
IMM167 Immune Deficiency Disease 78 1.177
29
P LNG064 Lung Cancer Susceptibility 3 77 1.177
30
P RTN008 Retinitis Pigmentosa 77 1.177
31
P LYN001 Lynch Syndrome 77 1.177
32
P PRK057 Parkinson Disease, Late-Onset 76 1.177
33
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 1.177
34
DFC004 Deficiency Anemia 75 1.177
35
P APL001 Aplastic Anemia 74 1.177
36
c MNN043 Meningioma, Familial 74 1.177
37
P RSP003 Respiratory Failure 74 1.177
38
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 1.177
39
BRN028 Brain Cancer 73 1.177
40
PLM129 Pulmonary Disease, Chronic Obstructive 73 1.177
41
SVR004 Severe Combined Immunodeficiency 73 1.177
42
ACR006 Aceruloplasminemia 73 1.177
43
LYM143 Lymphoma, Non-Hodgkin, Familial 72 1.177
44
P LFR001 Li-Fraumeni Syndrome 72 1.177
45
c LKM063 Leukemia, Chronic Myeloid 71 1.177
46
PRP027 Peripheral Vascular Disease 71 1.177
47
c MLT156 Multiple Endocrine Neoplasia, Type I 71 1.177
48
c MGR028 Migraine with or Without Aura 1 69 1.177
49
ADL002 Adult Syndrome 69 1.177
50
P FRG001 Fragile X Syndrome 68 1.177
51
P LKM062 Leukemia, Acute Lymphoblastic 68 1.177
52
P MYC084 Mycobacterium Tuberculosis 1 68 1.177
53
P CLC063 Celiac Disease 1 68 1.177
54
c FML021 Familial Hypercholesterolemia 68 1.177
55
SKN019 Skin Melanoma 67 1.177
56
P KBK002 Kabuki Syndrome 1 67 1.177
57
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 1.177
58
P ANG001 Angelman Syndrome 67 1.177
59
PSY004 Psychotic Disorder 67 1.177
60
P DRM053 Dermatitis, Atopic 66 1.177
61
CNN005 Connective Tissue Disease 66 1.177
62
P MCR115 Microvascular Complications of Diabetes 5 66 1.177
63
P DYS007 Dyskeratosis Congenita 66 1.177
64
P LYS001 Loeys-Dietz Syndrome 66 1.177
65
OMN001 Omenn Syndrome 66 1.177
66
CHD001 Chediak-Higashi Syndrome 66 1.177
67
P NRV007 Nervous System Disease 66 1.177
68
c PRD013 Periodic Fever, Familial, Autosomal Dominant 65 1.177
69
P ACR001 Aicardi-Goutieres Syndrome 65 1.177
70
RBR001 Roberts Syndrome 65 1.177
71
P TRC102 Trichothiodystrophy 1, Photosensitive 65 1.177
72
HTC003 Hutchinson-Gilford Progeria Syndrome 65 1.177
73
P BRL012 Bare Lymphocyte Syndrome, Type Ii 65 1.177
74
c WLM013 Wilms Tumor 1 65 1.177
75
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 64 1.177
76
TBC004 Tobacco Addiction 64 1.177
77
ALL026 Allergic Hypersensitivity Disease 64 1.177
78
RHB001 Rhabdoid Cancer 63 1.177
79
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 1.177
80
DGR001 Digeorge Syndrome 63 1.177
81
P NRN021 Neuronal Ceroid Lipofuscinosis 63 1.177
82
NRM005 Neuromuscular Disease 63 1.177
83
P CRN015 Cornelia De Lange Syndrome 63 1.177
84
SKN016 Skin Disease 63 1.177
85
c ACT068 Acute Cystitis 63 1.177
86
LPD008 Lipid Metabolism Disorder 62 1.177
87
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 62 1.177
88
P BCK002 Beckwith-Wiedemann Syndrome 62 1.177
89
c ALP101 Alpha-Thalassemia 62 1.177
90
P PLZ001 Pelizaeus-Merzbacher Disease 62 1.177
91
HMT002 Hematologic Cancer 62 1.177
92
MDD011 Mood Disorder 62 1.177
93
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 62 1.177
94
NTR005 Nutritional Deficiency Disease 61 1.177
95
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 61 1.177
96
c PNS012 Paine Syndrome 61 1.177
97
VRL011 Viral Infectious Disease 61 1.177
98
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 61 1.177
99
BRK001 Brooke-Spiegler Syndrome 60 1.177
100
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 1.177
101
P STS008 Sotos Syndrome 1 60 1.177
102
CFF002 Coffin-Lowry Syndrome 60 1.177
103
P HRD011 Hereditary Spherocytosis 60 1.177
104
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 1.177
105
SPP011 Suppression of Tumorigenicity 12 59 1.177
106
c DNG003 Dengue Disease 59 1.177
107
GRD007 Grade Iii Astrocytoma 59 1.177
108
P PRD006 Prader-Willi Syndrome 59 1.177
109
P BRS044 Breast Adenocarcinoma 59 1.177
110
PPT005 Peptic Ulcer Disease 58 1.177
111
THY025 Thymus Cancer 58 1.177
112
EYD002 Eye Disease 58 1.177
113
P ALC033 Alcohol Use Disorder 58 1.177
114
P MLN069 Melanoma, Uveal 58 1.177
115
BRS051 Breast Disease 58 1.177
116
WVR001 Weaver Syndrome 58 1.177
117
c LYS019 Loeys-Dietz Syndrome 1 57 1.177
118
P PRV006 Pervasive Developmental Disorder 57 1.177
119
P SCK004 Seckel Syndrome 57 1.177
120
c XRD022 Xeroderma Pigmentosum, Complementation Group D 57 1.177
121
P EXN002 Exanthem 57 1.177
122
DSS008 Disease of Mental Health 57 1.177
123
P PRP019 Peripheral Nervous System Disease 57 1.177
124
MNT002 Mental Depression 57 1.177
125
VRG001 Variegate Porphyria 56 1.177
126
WLF002 Wolf-Hirschhorn Syndrome 56 1.177
127
SPN041 Spinal Cord Disease 56 1.177
128
c AML044 Amelogenesis Imperfecta, Type Ig 56 1.177
129
ANS011 Anus Cancer 56 1.177
130
P ORL007 Oral Cavity Cancer 56 1.177
131
BCT022 Bacterial Infectious Disease 56 1.177
132
P CRD246 Cardiovascular System Disease 56 1.177
133
ANG005 Anogenital Venereal Wart 56 1.177
134
MTH009 Mouth Disease 56 1.177
135
RHM027 Rheumatic Disease 56 1.177
136
GST050 Gastrointestinal System Disease 56 1.177
137
HMN014 Human Immunodeficiency Virus Infectious Disease 55 1.177
138
c FML035 Familial Hyperlipidemia 55 1.177
139
c CRD183 Ceroid Lipofuscinosis, Neuronal, 2 55 1.177
140
c KLF004 Kleefstra Syndrome 1 55 1.177
141
P MRG008 Meier-Gorlin Syndrome 1 55 1.177
142
P FTL001 Fetal Alcohol Syndrome 55 1.177
143
OCL009 Ocular Cancer 55 1.177
144
ISL014 Isolated Growth Hormone Deficiency, Type Ia 55 1.177
145
GDP001 Goodpasture Syndrome 55 1.177
146
END002 Endometrioid Ovary Carcinoma 55 1.177
147
P SBS003 Substance Abuse 54 1.177
148
P SLV001 Silver-Russell Syndrome 54 1.177
149
END040 Endogenous Depression 54 1.177
150
c XRD030 Xeroderma Pigmentosum, Complementation Group C 54 1.177
151
ORP003 Oropharynx Cancer 54 1.177
152
LST001 Listeriosis 54 1.177
153
P HYP050 Hyperinsulinemic Hypoglycemia 54 1.177
154
c CNT035 Central Nervous System Disease 54 1.177
155
c FNC042 Fanconi Anemia, Complementation Group D2 54 1.177
156
c LKM070 Leukemia, Acute Monocytic 53 1.177
157
P XRD029 Xeroderma Pigmentosum, Complementation Group a 53 1.177
158
BRN038 Bronchial Disease 53 1.177
159
MST005 Mastitis 53 1.177
160
c XRD023 Xeroderma Pigmentosum, Complementation Group G 53 1.177
161
MCR165 Microphthalmia with Limb Anomalies 53 1.177
162
P OVR049 Ovarian Disease 53 1.177
163
ART140 Arteries, Anomalies of 53 1.177
164
c SPN291 Spinocerebellar Ataxia 7 53 1.177
165
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 53 1.177
166
P RTN018 Retinal Disease 52 1.177
167
P INT068 Intestinal Disease 52 1.177
168
ESP023 Esophageal Disease 52 1.177
169
SVR010 Severe Combined Immunodeficiency with Sensitivity to Ionizing Radiation 52 1.177
170
CMB003 Combined T Cell and B Cell Immunodeficiency 52 1.177
171
DMY004 Demyelinating Disease 52 1.177
172
P INS002 in Situ Carcinoma 52 1.177
173
FLT011 Felty Syndrome 52 1.177
174
SRS001 Serous Cystadenocarcinoma 52 1.177
175
TXC002 Toxic Encephalopathy 52 1.177
176
c PRM012 Primary Polycythemia 52 1.177
177
LYS002 Lysosomal Storage Disease 52 1.177
178
c FNC024 Fanconi Anemia, Complementation Group D1 52 1.177
179
OVR059 Ovary Adenocarcinoma 51 1.177
180
MSC190 Muscular Disease 51 1.177
181
WLS003 Wilson-Turner X-Linked Mental Retardation Syndrome 51 1.177
182
TLN003 Telangiectasis 51 1.177
183
c FNC025 Fanconi Anemia, Complementation Group J 51 1.177
184
BLD053 Blood Platelet Disease 51 1.177
185
c RBN022 Robinow Syndrome, Autosomal Recessive 1 51 1.177
186
SMT006 Somatoform Disorder 51 1.177
187
THY030 Thyroid Gland Disease 51 1.177
188
HRT011 Heart Septal Defect 50 1.177
189
FBR008 Fibrillary Astrocytoma 50 1.177
190
c CHR418 Chronic Leukemia 50 1.177
191
CCC002 Coccidiosis 50 1.177
192
c FNC029 Fanconi Anemia, Complementation Group I 50 1.177
193
FSC004 Fasciitis 50 1.177
194
CRV040 Cervix Carcinoma 50 1.177
195
RSP006 Respiratory System Disease 50 1.177
196
P NNT009 Neonatal Diabetes Mellitus 50 1.177
197
VGN020 Vaginal Disease 50 1.177
198
PRS034 Parasitic Helminthiasis Infectious Disease 49 1.177
199
c XRD032 Xeroderma Pigmentosum, Complementation Group B 49 1.177
200
RTN015 Retinal Cancer 49 1.177
201
PLC008 Placenta Disease 49 1.177
202
GST049 Gastrointestinal System Cancer 49 1.177
203
CLN045 Colonic Benign Neoplasm 49 1.177
204
LKC005 Leukocyte Adhesion Deficiency, Type Iii 49 1.177
205
NCR007 Necrotizing Fasciitis 49 1.177
206
BNR002 Bone Resorption Disease 48 1.177
207
BLD044 Bladder Disease 48 1.177
208
SCH074 Schuurs-Hoeijmakers Syndrome 48 1.177
209
BCT004 Bacteriuria 48 1.177
210
URN009 Urinary System Disease 48 1.177
211
P LYM024 Lymphatic System Disease 48 1.177
212
SLP001 Sleeping Sickness 48 1.177
213
ATS010 Autosomal Recessive Disease 48 1.177
214
LPD009 Lipid Storage Disease 48 1.177
215
RTN020 Retinal Vascular Disease 48 1.177
216
BNN003 Bone Inflammation Disease 48 1.177
217
P NRV006 Nervous System Cancer 48 1.177
218
P UTR058 Uterine Anomalies 48 1.177
219
c HRD026 Hereditary Ataxia 48 1.177
220
RCT017 Rectal Disease 48 1.177
221
SBS004 Substance Dependence 48 1.177
222
STM006 Stomach Disease 48 1.177
223
SPL012 Splenic Disease 48 1.177
224
c FNC046 Fanconi Anemia, Complementation Group P 47 1.177
225
SPH010 Sphingolipidosis 47 1.177
226
c PRM031 Primary Autosomal Recessive Microcephaly 47 1.177
227
P AML002 Amelogenesis Imperfecta 47 1.177
228
GRM005 Germ Cell Cancer 47 1.177
229
WRS002 Warsaw Breakage Syndrome 47 1.177
230
c BCT013 Bacterial Pneumonia 47 1.177
231
c FNC023 Fanconi Anemia, Complementation Group N 47 1.177
232
c NRP041 Neuropathy, Hereditary Sensory, Type Ie 47 1.177
233
c LRG017 Large Intestine Cancer 47 1.177
234
MCC002 Mucocutaneous Leishmaniasis 47 1.177
235
c MCR239 Microcephaly 5, Primary, Autosomal Recessive 46 1.177
236
P BLD051 Blood Coagulation Disease 46 1.177
237
PNC034 Pancreas Disease 46 1.177
238
P PNT019 Pontocerebellar Hypoplasia 46 1.177
239
c CNT033 Central Nervous System Cancer 46 1.177
240
c ACT076 Acute Myocarditis 46 1.177
241
CLN019 Colonic Disease 46 1.177
242
P BLR006 Biliary Tract Disease 46 1.177
243
CNG028 Congenital Hypoplastic Anemia 46 1.177
244
DRG013 Drug-Induced Lupus Erythematosus 46 1.177
245
END031 Endometrial Stromal Sarcoma 46 1.177
246
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 46 1.177
247
c INH020 Inherited Metabolic Disorder 46 1.177
248
ACT055 Actinomycosis 45 1.177
249
MLT018 Multiple Carboxylase Deficiency 45 1.177
250
ORC001 Orchitis 45 1.177
251
STR103 Streptococcus Pneumonia 45 1.177
252
HRP001 Herpangina 45 1.177
253
CRB027 Cerebellar Disease 45 1.177
254
IMM136 Immune System Disease 45 1.177
255
OHD004 Ohdo Syndrome 44 1.177
256
P END084 Endocrine System Disease 44 1.177
257
UTR033 Uterine Corpus Cancer 44 1.177
258
END035 Endocrine Gland Cancer 44 1.177
259
PLR022 Pleural Disease 44 1.177
260
CRB025 Carbohydrate Metabolic Disorder 44 1.177
261
c HYP840 Hypercholesterolemia, Familial, 4 44 1.177
262
CRS005 Crest Syndrome 44 1.177
263
NTM002 Nut Midline Carcinoma 44 1.177
264
LKD025 Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant 44 1.177
265
THR012 Thoracic Cancer 44 1.177
266
P HRT035 Heart Block, Congenital 44 1.177
267
P PHR004 Pharynx Cancer 44 1.177
268
CHR515 Chronic Atrial and Intestinal Dysrhythmia 44 1.177
269
INT253 Intestinal Benign Neoplasm 44 1.177
270
PRS042 Prostate Disease 44 1.177
271
c RTN047 Retinitis Pigmentosa 18 44 1.177
272
IMM104 Immunodeficiency with Hyper-Igm, Type 2 44 1.177
273
c FNC045 Fanconi Anemia, Complementation Group F 43 1.177
274
MSC072 Muscle Cancer 43 1.177
275
CMP007 Complement Component 5 Deficiency 43 1.177
276
ANL017 Anal Squamous Cell Carcinoma 43 1.177
277
P HYP073 Hypersensitivity Reaction Type Iv Disease 43 1.177
278
MTR010 Mature Teratoma 43 1.177
279
P ORF002 Orofacial Cleft 43 1.177
280
OVR063 Overnutrition 43 1.177
281
ANS012 Anus Disease 43 1.177
282
TST015 Testicular Disease 43 1.177
283
c CFF009 Coffin-Siris Syndrome 4 43 1.177
284
c SPH013 Spherocytosis, Type 1 43 1.177
285
BNM001 Bone Marrow Cancer 43 1.177
286
P PRM001 Primary Cutaneous Amyloidosis 43 1.177
287
P BLD036 Bile Duct Disease 43 1.177
288
TNS004 Tonsil Cancer 43 1.177
289
c SPH016 Spherocytosis, Type 4 43 1.177
290
P CRN024 Corneal Disease 43 1.177
291
c FTL006 Fetal Alcohol Spectrum Disorder 42 1.177
292
c CFF010 Coffin-Siris Syndrome 3 42 1.177
293
PRS036 Parasitic Protozoa Infectious Disease 42 1.177
294
c CFF007 Coffin-Siris Syndrome 2 42 1.177
295
P CLL015 Collagen Disease 42 1.177
296
PHY002 Physical Disorder 42 1.177
297
MXD023 Mixed Cell Type Cancer 42 1.177
298
CRB033 Cerebral Degeneration 42 1.177
299
IMM011 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 42 1.177
300
c TRN032 Transient Neonatal Diabetes Mellitus 42 1.177
301
LRY017 Laryngeal Disease 42 1.177
302
P HYP087 Hypotrichosis 42 1.177
303
LCN001 Lice Infestation 42 1.177
304
c PRM212 Primary Microcephaly 41 1.177
305
c RTN041 Retinitis Pigmentosa 11 41 1.177
306
c ATS307 Autosomal Recessive Cerebellar Ataxia 41 1.177
307
c HYP507 Hypotrichosis 1 41 1.177
308
P HRD018 Hair Disease 41 1.177
309
SLV003 Salivary Gland Disease 41 1.177
310
AMN002 Amino Acid Metabolic Disorder 40 1.177
311
MLR006 Male Reproductive Organ Cancer 40 1.177
312
c MYS052 Myasthenic Syndrome, Congenital, 10 40 1.177
313
GLC008 Glucose Metabolism Disease 40 1.177
314
c FNC052 Fanconi Anemia, Complementation Group T 40 1.177
315
LKC003 Leukocyte Disease 40 1.177
316
CHN004 Chondroblastoma 39 1.177
317
MNR003 Mineral Metabolism Disease 39 1.177
318
P SYN057 Syndromic Intellectual Disability 39 1.177
319
ESN002 Eosinophilia-Myalgia Syndrome 39 1.177
320
LMN006 Luminal Breast Carcinoma 39 1.177
321
IMM001 Immune-Complex Glomerulonephritis 39 1.177
322
P PRP021 Peripheral Nervous System Neoplasm 39 1.177
323
LNG030 Lung Adenoma 39 1.177
324
P UVS001 Uv-Sensitive Syndrome 39 1.177
325
c SPN335 Spinocerebellar Ataxia Type 1 with Axonal Neuropathy 38 1.177
326
MST004 Mast Cell Neoplasm 38 1.177
327
BLD054 Blood Protein Disease 38 1.177
328
c SPH015 Spherocytosis, Type 3 38 1.177
329
FML039 Female Reproductive System Disease 38 1.177
330
P NRM006 Neuromuscular Junction Disease 38 1.177
331
GND003 Gonadal Disease 38 1.177
332
OVR044 Ovarian Carcinosarcoma 38 1.177
333
BTN004 Biotin Deficiency 38 1.177
334
PLR006 Pleural Cancer 37 1.177
335
WST002 Western Equine Encephalitis 37 1.177
336
c HRD007 Hereditary Lymphedema 37 1.177
337
c RTN052 Retinitis Pigmentosa 23 37 1.177
338
CRV069 Cervix Disease 37 1.177
339
c RTN050 Retinitis Pigmentosa 20 37 1.177
340
XRD027 Xeroderma Pigmentosum Group E 37 1.177
341
ALP095 Alpha Thalassemia-X-Linked Intellectual Disability Syndrome 36 1.177
342
c ATS203 Autosomal Dominant Non-Syndromic Intellectual Disability 36 1.177
343
UVL010 Uveal Disease 36 1.177
344
UPP004 Upper Respiratory Tract Disease 36 1.177
345
RPR002 Reproductive System Disease 36 1.177
346
MLR007 Male Reproductive System Disease 36 1.177
347
RMN001 Rumination Disorder 36 1.177
348
INF039 Infratentorial Cancer 35 1.177
349
c ATM104 Autoimmune Vasculitis 35 1.177
350
P LNS003 Lens Disease 34 1.177
351
c HYP525 Hypotrichosis 2 34 1.177
352
BLD032 Bile Duct Adenocarcinoma 34 1.177
353
CNN004 Connective Tissue Cancer 33 1.177
354
END043 Endometrial Stromal Tumor 33 1.177
355
P HYP700 Hypomyelinating Leukodystrophy 33 1.177
356
OVR060 Ovary Epithelial Cancer 33 1.177
357
c SCH083 Schizophrenia 7 33 1.177
358
NSP003 Nasopharyngeal Disease 33 1.177
359
HRT008 Heart Conduction Disease 33 1.177
360
RSP004 Respiratory System Benign Neoplasm 32 1.177
361
P CHR084 Chromosomal Disease 32 1.177
362
P BND014 Bone Development Disease 32 1.177
363
CCL002 Cecal Disease 32 1.177
364
PTH001 Pthirus Pubis Infestation 32 1.177
365
MTR008 Mature B-Cell Neoplasm 32 1.177
366
GRM001 Germ Cell and Embryonal Cancer 32 1.177
367
THY026 Thymus Gland Disease 32 1.177
368
RSP005 Respiratory System Cancer 31 1.177
369
P LTT001 Lattice Corneal Dystrophy 31 1.177
370
SKL003 Skeletal Muscle Cancer 31 1.177
371
PRM025 Primary Bacterial Infectious Disease 31 1.177
372
EXT035 Extrinsic Cardiomyopathy 30 1.177
373
LYM023 Lymphatic System Cancer 30 1.177
374
c PRM023 Pre-Malignant Neoplasm 30 1.177
375
SPC003 Specific Developmental Disorder 30 1.177
376
c ATM007 Autoimmune Disease of Central Nervous System 30 1.177
377
CNT109 Central Nervous System Benign Neoplasm 30 1.177
378
BNR001 Bone Remodeling Disease 30 1.177
379
DGN003 Degeneration of Macula and Posterior Pole 30 1.177
380
INT084 Intrinsic Cardiomyopathy 29 1.177
381
CRD007 Cardiovascular Organ Benign Neoplasm 29 1.177
382
c AMY023 Amyotrophic Lateral Sclerosis Type 6 29 1.177
383
c CLL013 Cell Type Cancer 29 1.177
384
P NNS031 Non-Syndromic Intellectual Disability 28 1.177
385
c HRD202 Hereditary Lymphedema I 28 1.177
386
c RTN053 Retinitis Pigmentosa 24 28 1.177
387
PRS033 Parasitic Ectoparasitic Infectious Disease 28 1.177
388
P ACQ009 Acquired Metabolic Disease 28 1.177
389
ANS025 Anus Benign Neoplasm 28 1.177
390
FNC006 Functional Gastric Disease 28 1.177
391
ATM005 Autoimmune Disease of Musculoskeletal System 28 1.177
392
ATM015 Autoimmune Disease of Gastrointestinal Tract 27 1.177
393
CMM006 Commensal Bacterial Infectious Disease 27 1.177
394
END014 Endemic Typhus 27 1.177
395
P ATN003 Autonomic Nervous System Neoplasm 27 1.177
396
c ATS009 Autosomal Genetic Disease 27 1.177
397
c ATM014 Autoimmune Disease of Endocrine System 27 1.177
398
c CNG031 Congenital Nervous System Abnormality 27 1.177
399
END036 Endocrine Organ Benign Neoplasm 27 1.177
400
c CHR565 Chromosomal Deletion Syndrome 27 1.177
401
MLG076 Malignant Ovarian Surface Epithelial-Stromal Neoplasm 26 1.177
402
TTH005 Teeth Hard Tissue Disease 26 1.177
403
XLN228 X-Linked Recessive Disease 26 1.177
404
P SYN064 Syndromic X-Linked Intellectual Disability 25 1.177
405
MSC004 Muscle Tissue Disease 25 1.177
406
P BRN030 Brain Ependymoma 25 1.177
407
GST048 Gastrointestinal System Benign Neoplasm 24 1.177
408
CGN001 Cogan-Reese Syndrome 24 1.177
409
CLL012 Cell Type Benign Neoplasm 24 1.177
410
PLY179 Polyomavirus-Associated Nephropathy 23 1.177
411
ATM018 Autoimmune Disease of Urogenital Tract 22 1.177
412
P PRM016 Primary Optic Atrophy 22 1.177
413
c XLN230 X-Linked Monogenic Disease 20 1.177
414
ATR009 Atrophy of Testis 20 1.177
415
EPT024 Epithelial-Stromal Tgfbi Dystrophy 16 1.177
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