Search results for "myeloid malignancy, predisposition to"

The MalaCard for "myeloid malignancy, predisposition to" has been retired.
Searching MalaCards for entries containing "myeloid malignancy, predisposition to"

437 hits were found for 'myeloid malignancy, predisposition to'

# Family MCID Name MIFTS Score
1
PLT019 Platelet Disorder, Familial, with Associated Myeloid Malignancy 30 5.089
2
P LKM002 Leukemia 71 1.042
3
P MYL006 Myeloid Leukemia 66 0.928
4
c LKM061 Leukemia, Acute Myeloid 73 0.460
5
c ACT073 Acute Leukemia 60 0.424
6
c CHR064 Chronic Monocytic Leukemia 42 0.411
7
ACT118 Acute Non Lymphoblastic Leukemia 30 0.385
8
MLN008 Melanoma 62 0.380
9
P LYM118 Lymphoma 69 0.368
10
BNM001 Bone Marrow Cancer 51 0.353
11
MYL009 Myelodysplastic Syndrome 73 0.341
12
MRG013 Mirage Syndrome 29 0.341
13
SRC014 Sarcoma 66 0.325
14
PRM243 Primary Bone Cancer 29 0.319
15
P BRS047 Breast Cancer 100 0.311
16
HMT002 Hematologic Cancer 64 0.297
17
BNC003 Bone Cancer 58 0.294
18
P LKM068 Leukemia, Chronic Myeloid, Somatic 68 0.281
19
c CHR418 Chronic Leukemia 47 0.279
20
MYL031 Myeloproliferative Neoplasm 58 0.273
21
P HPT021 Hepatitis 69 0.258
22
P LYM026 Lymphoblastic Leukemia 62 0.254
23
P CHR562 Chronic Myelocytic Leukemia 41 0.248
24
P NRV006 Nervous System Cancer 60 0.246
25
END072 Endotheliitis 42 0.243
26
c PRM023 Pre-Malignant Neoplasm 41 0.243
27
PRS047 Prostatitis 56 0.243
28
HMT018 Hematopoietic Stem Cell Transplantation 41 0.231
29
P CLR023 Colorectal Cancer 97 0.222
30
P LNG032 Lung Cancer 95 0.221
31
MYL003 Myeloid Sarcoma 48 0.217
32
P THY032 Thyroiditis 54 0.215
33
P PNC044 Pancreatitis 61 0.212
34
P LYM033 Lymphoproliferative Syndrome 56 0.207
35
P ADN016 Adenocarcinoma 69 0.206
36
OCL009 Ocular Cancer 59 0.206
37
LYM067 Lymphoid Leukemia 44 0.205
38
LYM024 Lymphatic System Disease 52 0.205
39
P ART022 Arthritis 75 0.205
40
LYM023 Lymphatic System Cancer 33 0.205
41
P PRS040 Prostate Cancer 90 0.203
42
PRP021 Peripheral Nervous System Neoplasm 46 0.202
43
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.202
44
ACD009 Acid-Labile Subunit, Deficiency of 45 0.196
45
c CHR090 Chronic Lymphocytic Leukemia 76 0.194
46
KDS001 Kid Syndrome 53 0.192
47
ADL002 Adult Syndrome 52 0.190
48
CHL071 Child Syndrome 58 0.189
49
CSY001 C Syndrome 50 0.189
50
LYM019 Lymphosarcoma 53 0.189
51
ORL011 Oral Cancer 56 0.185
52
P ACT074 Acute Lymphocytic Leukemia 56 0.184
53
P MLT019 Multiple Myeloma 83 0.183
54
BRT030 Birth Defects 43 0.182
55
WLL006 Wells Syndrome 59 0.179
56
P MDL005 Medulloblastoma 77 0.179
57
GDS001 Good Syndrome 44 0.179
58
P ORL007 Oral Cavity Cancer 59 0.178
59
c LKM062 Leukemia, Acute Lymphoblastic 64 0.177
60
P OVR042 Ovarian Cancer 76 0.176
61
P HPT023 Hepatocellular Carcinoma 92 0.176
62
DFC004 Deficiency Anemia 64 0.175
63
ADN018 Adenoma 58 0.175
64
P RHM011 Rheumatoid Arthritis 89 0.174
65
c CLL013 Cell Type Cancer 46 0.174
66
SQM006 Squamous Cell Carcinoma 70 0.174
67
P BCL006 B-Cell Lymphomas 65 0.170
68
EWN003 Ewing Sarcoma 66 0.168
69
c ADL052 Adult Acute Lymphocytic Leukemia 44 0.168
70
TST021 Testicular Germ Cell Tumor 69 0.167
71
CHL061 Childhood Leukemia 49 0.167
72
ACT113 Acute Myeloblastic Leukemia with Maturation 37 0.166
73
ACT114 Acute Myeloblastic Leukemia Without Maturation 29 0.166
74
THR024 Thrombosis 57 0.165
75
P HRT032 Heart Disease 75 0.165
76
SNS023 Sensory System Cancer 43 0.163
77
P TCL004 T-Cell Leukemia 47 0.161
78
GST053 Gastric Cancer 78 0.161
79
P RNL014 Renal Cell Carcinoma 82 0.159
80
VSC006 Vascular Cancer 51 0.158
81
GRM001 Germ Cell and Embryonal Cancer 36 0.157
82
P PLR004 Pleuropulmonary Blastoma 65 0.156
83
BND014 Bone Development Disease 40 0.156
84
ACR002 Acrocapitofemoral Dysplasia 33 0.156
85
P GST049 Gastrointestinal System Cancer 60 0.155
86
P CRV039 Cervicitis 45 0.154
87
P PNC035 Pancreatic Cancer 87 0.154
88
BNL002 Bone Lymphoma 32 0.154
89
ISC004 Ischemia 61 0.153
90
P PNM007 Pneumonia 68 0.153
91
CRB009 Cerebritis 39 0.153
92
P OBS005 Obesity 92 0.152
93
c ADL017 Adult T-Cell Leukemia 60 0.152
94
NRL004 Neuroleptic Malignant Syndrome 41 0.150
95
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.149
96
HRT007 Heart Cancer 46 0.146
97
SKN016 Skin Disease 66 0.145
98
P KDN017 Kidney Cancer 65 0.144
99
P HRT017 Heart Tumor 32 0.143
100
P BLD051 Blood Coagulation Disease 42 0.143
101
c ADL079 Adult Heart Tumor 16 0.142
102
P AST005 Asthma 82 0.142
103
LYM115 Lymphoma, Non-Hodgkin 63 0.141
104
P THR014 Thrombocytopenia 64 0.140
105
c HPT001 Hepatitis C 68 0.138
106
ALN001 Aland Island Eye Disease 45 0.138
107
PRP027 Peripheral Vascular Disease 69 0.137
108
PRM151 Primary Bone Lymphoma 26 0.137
109
FRB001 Farber Lipogranulomatosis 53 0.137
110
P NRB001 Neuroblastoma 70 0.135
111
CRD118 Cardiovascular Cancer 44 0.134
112
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.134
113
P SPS003 Spastic Diplegia 52 0.134
114
TBR010 Tuberculosis 70 0.133
115
CNT018 Central Nervous System Leukemia 37 0.132
116
NRN002 Neuronitis 41 0.132
117
BRN028 Brain Cancer 70 0.132
118
ALR002 Al-Raqad Syndrome 36 0.131
119
P SKN013 Skin Benign Neoplasm 43 0.131
120
NTR005 Nutritional Deficiency Disease 36 0.131
121
RTN023 Retinitis 50 0.130
122
c LKM056 Leukemia, Chronic Lymphocytic 2 21 0.130
123
P MYC007 Myocardial Infarction 79 0.130
124
CNN005 Connective Tissue Disease 62 0.128
125
c LYM107 Lymphoproliferative Syndrome 2 50 0.127
126
P MNN013 Meningitis 67 0.127
127
c LKM004 Leukemia, B-Cell, Chronic 24 0.127
128
P ESP024 Esophagitis 61 0.126
129
c LYM106 Lymphoproliferative Syndrome 1 32 0.126
130
MXD023 Mixed Cell Type Cancer 45 0.125
131
INT253 Intestinal Benign Neoplasm 47 0.125
132
MTH009 Mouth Disease 61 0.124
133
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.123
134
HDG012 Hodgkin Lymphoma 77 0.123
135
NRN004 Neuroendocrine Tumor 56 0.123
136
P CHR084 Chromosomal Disease 32 0.122
137
P LPS004 Lupus Erythematosus 64 0.121
138
ATP002 Atopy 66 0.121
139
CRC006 Carcinoid Syndrome 52 0.121
140
P ENC004 Encephalitis 63 0.121
141
ANR040 Aneurysm 57 0.118
142
P NRF002 Neurofibromatosis 71 0.118
143
FML039 Female Reproductive System Disease 48 0.118
144
DRM006 Dermatitis 66 0.118
145
P INF037 Inflammatory Bowel Disease 63 0.118
146
c PND001 Pain Disorder 54 0.118
147
GLM004 Gliomatosis Cerebri 49 0.117
148
CNT010 Central Nervous System Hematologic Cancer 18 0.117
149
ADM013 Adamantinoma of Long Bones 57 0.117
150
P MYP004 Myopathy 67 0.116
151
ACQ007 Acquired Immunodeficiency Syndrome 60 0.116
152
c SYS001 Systemic Lupus Erythematosus 86 0.114
153
ART111 Artery Disease 55 0.113
154
MDS022 Mediastinitis 41 0.113
155
P OVR049 Ovarian Disease 56 0.113
156
LRN003 Learning Disability 49 0.112
157
END035 Endocrine Gland Cancer 49 0.112
158
P APL001 Aplastic Anemia 75 0.112
159
GST019 Gastrointestinal Stromal Tumor 73 0.111
160
PRD011 Proud Syndrome 42 0.111
161
CLT003 Colitis 60 0.110
162
P SML001 Small Cell Carcinoma 56 0.110
163
SML033 Small Cell Cancer of the Lung, Somatic 54 0.109
164
FML038 Female Reproductive Organ Cancer 50 0.109
165
RDT005 Radiation Induced Cancer 28 0.109
166
BRN038 Bronchial Disease 51 0.109
167
P CRD011 Cardiomyopathy 68 0.109
168
P CHR345 Chronic Pain 50 0.109
169
P CRN211 Coronary Artery Disease 74 0.108
170
P KDN018 Kidney Disease 66 0.108
171
RPR002 Reproductive System Disease 41 0.108
172
CNG034 Congestive Heart Failure 72 0.108
173
P ASP006 Aspergillosis 61 0.107
174
VSC007 Vascular Disease 67 0.107
175
P CNN004 Connective Tissue Cancer 40 0.107
176
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 56 0.107
177
c CNN010 Connective Tissue Benign Neoplasm 32 0.106
178
PRM025 Primary Bacterial Infectious Disease 41 0.106
179
PRM097 Primary Immunodeficiency Disease 60 0.106
180
ATH003 Atherosclerosis 65 0.106
181
DWN001 Down Syndrome 66 0.106
182
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.105
183
SFT003 Soft Tissue Sarcoma 57 0.105
184
P SCH015 Schizophrenia 77 0.105
185
c SML023 Small Cell Lung Cancer, Adult 15 0.105
186
PRP019 Peripheral Nervous System Disease 55 0.104
187
P ESS003 Essential Thrombocythemia 70 0.104
188
PRS042 Prostate Disease 52 0.104
189
CLV009 Clove Syndrome, Somatic 41 0.103
190
RCT018 Rectal Neoplasm 54 0.102
191
P INT068 Intestinal Disease 60 0.102
192
LNG099 Lung Disease 64 0.102
193
SXL003 Sexual Disorder 42 0.102
194
TMR010 Tumor Predisposition Syndrome 47 0.102
195
c HPT073 Hepatitis C Virus 73 0.101
196
PNC034 Pancreas Disease 58 0.101
197
PRL032 Perlman Syndrome 50 0.101
198
c BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.101
199
DDN006 Duodenitis 42 0.101
200
MLR004 Malaria 83 0.100
201
NSY001 N Syndrome 36 0.100
202
c PNC106 Pancreatic Agenesis 1 37 0.100
203
MLR007 Male Reproductive System Disease 34 0.100
204
MCR004 Macroglobulinemia 50 0.100
205
WST001 West Syndrome 57 0.099
206
RHB003 Rhabdomyosarcoma 57 0.099
207
WLM007 Wilms Tumor Susceptibility-5 63 0.099
208
THR004 Thrombocytosis 55 0.098
209
MST016 Mesothelioma, Somatic 51 0.098
210
MCS002 Mucositis 55 0.098
211
P FLL037 Follicular Lymphoma 70 0.097
212
THY028 Thyroid Cancer 69 0.097
213
PLR022 Pleural Disease 51 0.097
214
P CRN178 Coronary Heart Disease 6 21 0.097
215
DMN002 Dementia 65 0.096
216
P PSR002 Psoriasis 61 0.096
217
PLR006 Pleural Cancer 44 0.095
218
BCK006 Back Pain 43 0.095
219
CNT098 Central Core Disease 65 0.095
220
RNL101 Renal Cell Carcinoma, Papillary 63 0.095
221
MLR006 Male Reproductive Organ Cancer 43 0.095
222
VSC001 Vascular Myelopathy 23 0.094
223
HRT029 Heart Tumor of the Child 15 0.094
224
P ATX004 Ataxia 53 0.094
225
P RTN024 Retinoblastoma 74 0.094
226
c FML108 Familial Breast Cancer 57 0.094
227
ISC006 Ischemic Heart Disease 68 0.093
228
c HYP595 Hypertension, Essential 69 0.093
229
c CLR085 Colorectal Cancer 1 45 0.093
230
c CLR079 Colorectal Cancer 2 29 0.093
231
c NRF018 Neurofibromatosis, Type 1 67 0.093
232
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.093
233
STM006 Stomach Disease 50 0.092
234
FML037 Female Breast Cancer 50 0.091
235
END030 End Stage Renal Failure 55 0.090
236
P GLM007 Glomerulonephritis 59 0.090
237
GND003 Gonadal Disease 39 0.090
238
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.090
239
c INV001 Invasive Aspergillosis 47 0.089
240
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.089
241
CRH001 Crohn's Disease 75 0.088
242
ULC004 Ulcerative Colitis 76 0.088
243
P UTR038 Uterine Disease 37 0.088
244
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.087
245
P LRY019 Laryngitis 54 0.087
246
c CLR075 Colorectal Cancer 3 28 0.087
247
SPC003 Specific Developmental Disorder 38 0.087
248
LYM127 Lymphatic Malformations 39 0.086
249
c CHR089 Chronic Kidney Failure 66 0.086
250
P END044 Endometriosis 66 0.085
251
P ATR011 Atrial Fibrillation 66 0.085
252
c INH020 Inherited Metabolic Disorder 49 0.084
253
HRY003 Hairy Cell Leukemia 57 0.084
254
CYS001 Cystic Fibrosis 83 0.084
255
PRP030 Purpura 58 0.084
256
c PRS116 Prostate Cancer 1 37 0.084
257
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.084
258
TST014 Testicular Cancer 53 0.084
259
P PNC001 Pancytopenia 52 0.082
260
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.081
261
P UVT001 Uveitis 58 0.081
262
CLN015 Colon Adenocarcinoma 50 0.081
263
P HRP006 Herpes Simplex 65 0.080
264
MSC072 Muscle Cancer 49 0.080
265
CHR008 Choroiditis 44 0.079
266
LMY002 Leiomyoma 54 0.078
267
P LFR001 Li-Fraumeni Syndrome 75 0.078
268
P GRV001 Graves' Disease 59 0.078
269
TTH006 Tooth Disease 52 0.078
270
P PRD008 Periodontitis 63 0.078
271
GLL018 Gallbladder Cancer 63 0.078
272
GNR004 Generalized Anxiety Disorder 51 0.077
273
BRN071 Brain Injury 52 0.077
274
OVR094 Ovarian Epithelial Cancer 43 0.077
275
UTR033 Uterine Corpus Cancer 49 0.076
276
EXF001 Exfoliation Syndrome 57 0.076
277
SPN051 Spondylitis 51 0.075
278
P OST012 Osteoarthritis 83 0.075
279
c PNC094 Pancreatic Cancer 1 27 0.075
280
P PLN008 Peeling Skin Syndrome 45 0.075
281
c WLM005 Wilms Tumor 2 20 0.074
282
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.074
283
P THL005 Thalassemia 64 0.074
284
P RTN022 Retinal Vein Occlusion 38 0.074
285
P LPR003 Leprosy 69 0.074
286
YNG002 Young Syndrome 26 0.073
287
ART016 Aortic Aneurysm 69 0.073
288
P ATX030 Ataxia-Telangiectasia 77 0.073
289
PHR003 Pharyngitis 56 0.072
290
MLN013 Melanoma Metastasis 40 0.072
291
OTT002 Otitis Media 66 0.072
292
P ATP001 Atopic Dermatitis 62 0.072
293
P CHL066 Cholangitis 42 0.071
294
P CNT005 Central Nervous System Lymphoma 53 0.071
295
P WLD002 Waldenstrom Macroglobulinemia 58 0.071
296
c FML303 Familial/multiple Cancer 14 0.070
297
P RHN004 Rhinitis 60 0.070
298
THR013 Thoracic Outlet Syndrome 50 0.069
299
EMB004 Embryonal Carcinoma 57 0.069
300
VSC047 Vascular Malformation 45 0.069
301
VSC009 Vascular Skin Disease 19 0.068
302
c PRM226 Primary Central Nervous System Lymphoma 49 0.068
303
P SML016 Small Intestine Cancer 52 0.068
304
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.068
305
SYN036 Syncope 47 0.068
306
STT009 Sutton Disease 2 18 0.067
307
PRR002 Pure Red-Cell Aplasia 47 0.067
308
ALL003 Allergic Rhinitis 63 0.067
309
P PLY019 Polyneuropathy 56 0.067
310
P END033 Endocarditis 54 0.067
311
TTR011 Tetraploidy 41 0.067
312
c PLN018 Peeling Skin Syndrome 2 40 0.067
313
P ALX003 Alexander Disease 63 0.067
314
PLM001 Pulmonary Tuberculosis 67 0.066
315
P MCR129 Microvascular Complications of Diabetes 1 54 0.066
316
SCK003 Sickle Cell Anemia 71 0.066
317
c PLN021 Peeling Skin Syndrome 3 29 0.065
318
UPP004 Upper Respiratory Tract Disease 46 0.065
319
OVR069 Ovarian Germ Cell Tumor 24 0.065
320
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.065
321
BNF002 Bone Fracture 50 0.064
322
HRT003 Heart Lymphoma 30 0.063
323
P GST044 Gastritis 56 0.063
324
CNT067 Central Cord Syndrome 23 0.063
325
ACT017 Acute Chest Syndrome 48 0.063
326
c CNT016 Central Retinal Vein Occlusion 36 0.063
327
TRM010 Traumatic Brain Injury 52 0.063
328
c PLN017 Peeling Skin Syndrome 1 34 0.063
329
c FNC027 Fanconi Anemia, Complementation Group a 71 0.063
330
BLM001 Bloom Syndrome 63 0.062
331
P LYM025 Lymphedema 61 0.062
332
ERY003 Erythema Multiforme 55 0.062
333
KWS002 Kawasaki Disease 70 0.062
334
AND005 Androgen Insensitivity Syndrome, Mild 16 0.061
335
TNS005 Tonsillitis 57 0.061
336
SHW002 Shwachman-Diamond Syndrome 61 0.061
337
BRN002 Bronchiolitis 56 0.061
338
c BCT007 Bacterial Meningitis 54 0.061
339
c INF086 Inflammatory Bowel Disease 3 38 0.061
340
c ATM011 Autoimmune Hepatitis 60 0.061
341
P MTC069 Mitochondrial Disorders 53 0.061
342
SXD001 Sex Differentiation Disease 38 0.060
343
PRS039 Prostate Adenocarcinoma 46 0.060
344
P THR015 Thrombophilia 59 0.060
345
P FNC004 Fanconi Syndrome 49 0.060
346
GST014 Gastrointestinal Lymphoma 31 0.059
347
TCL003 T Cell Deficiency 45 0.058
348
SNG003 Single Ventricular Heart 22 0.057
349
LRG008 Large Granular Lymphocyte Leukemia 39 0.057
350
BCL002 B Cell Deficiency 49 0.057
351
MDY005 Mody, Type I 30 0.056
352
c WLM011 Wilms Tumor 6 19 0.056
353
c RNL034 Renal Cell Carcinoma 4 18 0.056
354
P MYS003 Myasthenia Gravis 67 0.056
355
EPD001 Epidermodysplasia Verruciformis 50 0.056
356
BLM002 Bulimia Nervosa 52 0.055
357
CLN044 Colon Adenoma 44 0.055
358
ADR038 Adermatoglyphia 46 0.055
359
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.054
360
LPR001 Lepromatous Leprosy 50 0.054
361
ADR005 Adrenal Carcinoma 57 0.054
362
P SLV002 Salivary Gland Cancer 61 0.054
363
CHL067 Cholecystitis 57 0.054
364
HPT022 Hepatoblastoma 55 0.054
365
P BCK002 Beckwith-Wiedemann Syndrome 56 0.053
366
MXD005 Mixed Connective Tissue Disease 62 0.053
367
P ANT006 Antiphospholipid Syndrome 56 0.053
368
BRS001 Breast Lymphoma 32 0.053
369
c CNG031 Congenital Nervous System Abnormality 37 0.052
370
BLL006 Bullous Pemphigoid 59 0.052
371
CNT045 Central Nervous System Sarcoma 16 0.052
372
CHR066 Chronic Fatigue Syndrome 64 0.051
373
ABL002 Ablepharon-Macrostomia Syndrome 57 0.051
374
HYP037 Hyperhomocysteinemia 50 0.051
375
CNG028 Congenital Hypoplastic Anemia 48 0.051
376
RNL097 Renal Artery Disease 43 0.050
377
FCT003 Factor X Deficiency 61 0.050
378
P DMN001 Diamond-Blackfan Anemia 69 0.050
379
P TST026 Testicular Germ Cell Cancer 39 0.050
380
P NJM001 Nijmegen Breakage Syndrome 67 0.049
381
c ANT034 Anterior Uveitis 48 0.049
382
P HRD018 Hair Disease 51 0.049
383
ASP003 Aseptic Meningitis 51 0.049
384
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.049
385
P FCL005 Focal Segmental Glomerulosclerosis 60 0.049
386
NNH003 Non-Hodgkin Lymphoma, Childhood 12 0.049
387
c SVR001 Severe Acute Respiratory Syndrome 57 0.048
388
RNL077 Renal Fibrosis 47 0.048
389
OVR104 Ovarian Melanoma 36 0.048
390
WRN001 Werner Syndrome 67 0.048
391
KDN020 Kidney Cancer, Childhood 11 0.048
392
c OVR058 Ovarian Small Cell Carcinoma 36 0.048
393
P FML187 Familial Hypertension 38 0.047
394
c INH015 Inherited Acute Myeloid Leukemia 25 0.047
395
c NRB015 Neuroblastoma 2 28 0.046
396
P GND004 Gonadal Dysgenesis 51 0.046
397
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.046
398
SKN021 Skin Sarcoma 25 0.046
399
KDN019 Kidney Sarcoma 31 0.045
400
c HRD009 Hereditary Wilms' Tumor 36 0.045
401
MTG002 Mutagen Sensitivity 36 0.044
402
c PRM200 Primary Fanconi Syndrome 24 0.044
403
OVR029 Ovarian Hyperstimulation Syndrome 61 0.044
404
WGR001 Wagr Syndrome 53 0.043
405
c VRL005 Viral Pneumonia 42 0.043
406
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 47 0.042
407
MDY004 Mody, Type Iii 34 0.042
408
DYS164 Dyskeratosis Congenita, X-Linked 44 0.042
409
HRF001 Hair Follicle Neoplasm 32 0.041
410
P RTH001 Rothmund-Thomson Syndrome 55 0.041
411
PRS008 Prostate Small Cell Carcinoma 29 0.041
412
CRS001 Crescentic Glomerulonephritis 42 0.041
413
RNL021 Renal Tubular Transport Disease 32 0.040
414
SFT004 Soft Tissue Sarcoma Childhood 12 0.040
415
HND003 Hand-Foot-Uterus Syndrome 50 0.040
416
CYS036 Cystinosis, Nephropathic 41 0.040
417
LTX001 Latex Allergy 38 0.040
418
P FML321 Familial Stomach Cancer 13 0.040
419
P ESN008 Eosinophilic Pneumonia 51 0.039
420
RNL025 Renal Hypoplasia 42 0.039
421
OVR050 Ovarian Embryonal Carcinoma 36 0.039
422
c FNC024 Fanconi Anemia, Complementation Group D1 28 0.039
423
HRT010 Heart Sarcoma 37 0.038
424
c DMN023 Diamond-Blackfan Anemia 1 38 0.037
425
c CHR576 Chronic Beryllium Disease 41 0.037
426
NRC007 Neuroectodermal Endocrine Syndrome 19 0.036
427
PLM139 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 1 27 0.035
428
c DMN005 Diamond-Blackfan Anemia 2 22 0.035
429
SCH002 Schnitzler Syndrome 51 0.034
430
P OVR075 Ovarian Dysgenesis 1 32 0.034
431
c OVR076 Ovarian Dysgenesis 2 31 0.034
432
c FNC042 Fanconi Anemia, Complementation Group D2 37 0.034
433
PNC059 Punctate Inner Choroidopathy 27 0.034
434
DDX002 Ddx41-Related Susceptibility to Familial Myeloproliferative/lymphoproliferative Neoplasms 13 0.033
435
P RNL100 Renal Hypodysplasia/aplasia 1 53 0.032
436
P FML153 Familial Wilms Tumor 17 0.031
437
MLN012 Melanoma and Neural System Tumor Syndrome 24 0.027