Search results for erythrocytosis

299 hits were found for erythrocytosis

# Family MCID Name MIFTS Score
1
ERY045 Erythrocytosis, Somatic 46 8.975
2
P ERY048 Erythrocytosis, Familial, 2 42 6.356
3
c PRM012 Primary Polycythemia 52 5.438
4
c ERY031 Erythrocytosis, Familial, 3 17 4.936
5
c ERY032 Erythrocytosis, Familial, 4 16 4.936
6
ERY044 Erythrocytosis Due to Bisphosphoglycerate Mutase Deficiency 19 4.035
7
TMP008 Tempi Syndrome 22 2.881
8
ATS075 Autosomal Recessive Secondary Polycythemia Not Associated with Vhl Gene 5 2.818
9
PLY125 Polycythemia Vera, Somatic 63 2.049
10
ERY007 Erythropoietin Polycythemia 15 2.025
11
STR007 Stress Polycythemia 19 1.993
12
c ATS209 Autosomal Dominant Secondary Polycythemia 15 1.993
13
PSD044 Pseudopolycythaemia 9 1.993
14
MLT106 Multiple Paragangliomas Associated with Polycythemia 7 1.993
15
P PLY018 Polycythemia 58 0.163
16
HMN009 Hemangioblastoma 45 0.109
17
c CHR546 Chronic Mountain Sickness 40 0.102
18
THR004 Thrombocytosis 55 0.094
19
MYM001 Myoma 52 0.094
20
P HPT023 Hepatocellular Carcinoma 92 0.086
21
P HPT021 Hepatitis 69 0.086
22
P PRG013 Paraganglioma 54 0.086
23
P PHC003 Pheochromocytoma 71 0.077
24
P THL005 Thalassemia 64 0.077
25
ADN018 Adenoma 58 0.077
26
THR024 Thrombosis 57 0.077
27
RNL007 Renal Tubular Acidosis 50 0.077
28
NPH003 Nephrocalcinosis 48 0.077
29
GST019 Gastrointestinal Stromal Tumor 73 0.067
30
P HMC003 Hemochromatosis 72 0.067
31
HYP266 Hypoxia 56 0.067
32
P ACT105 Acute Mountain Sickness 52 0.067
33
HYP043 Hyperandrogenism 47 0.067
34
P RNL014 Renal Cell Carcinoma 82 0.054
35
P HRT032 Heart Disease 75 0.054
36
P APL001 Aplastic Anemia 75 0.054
37
P LKM002 Leukemia 71 0.054
38
P ESS003 Essential Thrombocythemia 70 0.054
39
c HPT001 Hepatitis C 68 0.054
40
P MYL005 Myelofibrosis 67 0.054
41
HYP056 Hypoglycemia 61 0.054
42
MYL031 Myeloproliferative Neoplasm 58 0.054
43
LMY002 Leiomyoma 54 0.054
44
P HYP014 Hyperuricemia 50 0.054
45
HPT074 Hepatic Adenoma, Somatic 50 0.054
46
P RNL017 Renal Oncocytoma 47 0.054
47
SPL018 Splenomegaly 44 0.054
48
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.054
49
CRB009 Cerebritis 39 0.054
50
c SPR094 Sporadic Pheochromocytoma 36 0.054
51
HRS011 Horseshoe Kidney 33 0.054
52
HNM002 Hinman Syndrome 25 0.054
53
P MLT019 Multiple Myeloma 83 0.038
54
STR067 Stroke, Ischemic 75 0.038
55
INS024 Insulin-Like Growth Factor I 75 0.038
56
c LKM061 Leukemia, Acute Myeloid 73 0.038
57
MYL009 Myelodysplastic Syndrome 73 0.038
58
CNG034 Congestive Heart Failure 72 0.038
59
P RSP003 Respiratory Failure 71 0.038
60
P NRF002 Neurofibromatosis 71 0.038
61
P NRB001 Neuroblastoma 70 0.038
62
P ADN016 Adenocarcinoma 69 0.038
63
c MLT136 Multiple Endocrine Neoplasia 1 69 0.038
64
P DMN001 Diamond-Blackfan Anemia 69 0.038
65
VNH007 Von Hippel-Lindau Syndrome 69 0.038
66
P PNM007 Pneumonia 68 0.038
67
P LKM068 Leukemia, Chronic Myeloid, Somatic 68 0.038
68
LVR012 Liver Cirrhosis 67 0.038
69
c NRF018 Neurofibromatosis, Type 1 67 0.038
70
P KDN018 Kidney Disease 66 0.038
71
MYC006 Mycosis Fungoides 66 0.038
72
P KDN017 Kidney Cancer 65 0.038
73
P AMY004 Amyloidosis 65 0.038
74
P CWD001 Cowden Disease 64 0.038
75
c MLT024 Multiple Endocrine Neoplasia Iia 64 0.038
76
HMT002 Hematologic Cancer 64 0.038
77
DFC004 Deficiency Anemia 64 0.038
78
P THR014 Thrombocytopenia 64 0.038
79
c HMP029 Hemophilia a 63 0.038
80
P HYP098 Hypereosinophilic Syndrome 63 0.038
81
P MDL022 Medullary Thyroid Carcinoma, Familial 63 0.038
82
P HML002 Hemolytic Anemia 62 0.038
83
VNW001 Von Willebrand's Disease 61 0.038
84
P RCK004 Rickets 61 0.038
85
PLM033 Pulmonary Embolism 60 0.038
86
c SYS004 Systemic Mastocytosis 60 0.038
87
HYP020 Hyperprolactinemia 60 0.038
88
c ACT073 Acute Leukemia 60 0.038
89
LKM066 Leukemia, Acute Myelomonocytic, Somatic, Somatic 60 0.038
90
P THR015 Thrombophilia 59 0.038
91
P NTR004 Neutropenia 59 0.038
92
P INT001 Intrahepatic Cholestasis 59 0.038
93
CHL068 Cholestasis 59 0.038
94
RSP006 Respiratory System Disease 58 0.038
95
P BRS044 Breast Adenocarcinoma 58 0.038
96
P HYP069 Hyperparathyroidism 58 0.038
97
P HMP007 Hemophilia 57 0.038
98
FCT006 Factor V Deficiency 57 0.038
99
CHL067 Cholecystitis 57 0.038
100
c CWD006 Cowden Syndrome 1 57 0.038
101
HRY003 Hairy Cell Leukemia 57 0.038
102
PBL001 Piebaldism 57 0.038
103
P HMR003 Hemorrhagic Disease 57 0.038
104
UTR039 Uterine Fibroid 57 0.038
105
SNS001 Sensorineural Hearing Loss 57 0.038
106
P HYP613 Hypophosphatemic Rickets 57 0.038
107
P MST009 Mastocytosis 56 0.038
108
PTT006 Pituitary Adenoma 56 0.038
109
P MLT074 Multiple Endocrine Neoplasia 56 0.038
110
NRN004 Neuroendocrine Tumor 56 0.038
111
DSM004 Desmoid Tumor 56 0.038
112
c HYP615 Hyperparathyroidism, Familial Primary 56 0.038
113
CHR285 Chronic Myelomonocytic Leukemia 56 0.038
114
c SVR003 Severe Congenital Neutropenia 56 0.038
115
P PND002 Pendred Syndrome 55 0.038
116
P HYP076 Hyperthyroidism 55 0.038
117
MGK001 Megakaryocytic Leukemia 55 0.038
118
LMY005 Leiomyomatosis and Renal Cell Cancer 55 0.038
119
HPT022 Hepatoblastoma 55 0.038
120
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.038
121
END030 End Stage Renal Failure 55 0.038
122
P HYP345 Hyper-Ige Recurrent Infection Syndrome 54 0.038
123
c THR092 Thrombophilia Due to Thrombin Defect 54 0.038
124
c THR082 Thrombophilia Due to Activated Protein C Resistance 54 0.038
125
c RNL003 Renal Clear Cell Carcinoma 54 0.038
126
P HYP620 Hypoprothrombinemia 54 0.038
127
PRG097 Paragangliomas 1, with or Without Deafness 54 0.038
128
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.038
129
KDS001 Kid Syndrome 53 0.038
130
P PLY014 Polycystic Kidney Disease 53 0.038
131
CLR030 Clear Cell Renal Cell Carcinoma 53 0.038
132
THR016 Thrombophlebitis 53 0.038
133
FCT022 Factor Xi Deficiency, Autosomal Recessive 53 0.038
134
DST005 Diastrophic Dysplasia 53 0.038
135
P PNC001 Pancytopenia 52 0.038
136
CRC006 Carcinoid Syndrome 52 0.038
137
P ERY008 Erythromelalgia 51 0.038
138
BNM001 Bone Marrow Cancer 51 0.038
139
MTC020 Mitochondrial Complex Ii Deficiency 50 0.038
140
MST017 Mast Cell Disease 50 0.038
141
THR013 Thoracic Outlet Syndrome 50 0.038
142
END035 Endocrine Gland Cancer 49 0.038
143
CTN014 Cutaneous Mastocytosis 49 0.038
144
INN002 Inner Ear Disease 49 0.038
145
c ALM001 Al Amyloidosis 49 0.038
146
P FNC004 Fanconi Syndrome 49 0.038
147
SMT003 Somatostatinoma 48 0.038
148
PRT029 Parathyroid Adenoma 48 0.038
149
CHL004 Cholelithiasis 48 0.038
150
P AFB001 Afibrinogenemia 48 0.038
151
ATY042 Atypical Chronic Myeloid Leukemia 48 0.038
152
ACT098 Acute Erythroid Leukemia 47 0.038
153
VND001 Vein Disease 47 0.038
154
ERY021 Erythrokeratodermia Variabilis Et Progressiva 47 0.038
155
LYM116 Lymph Node Disease 47 0.038
156
HYD002 Hydronephrosis 47 0.038
157
PLC003 Placental Site Trophoblastic Tumor 47 0.038
158
LYM051 Lymphomatoid Granulomatosis 47 0.038
159
HYP108 Hyperparathyroidism-Jaw Tumor Syndrome 47 0.038
160
PST095 Post-Thrombotic Syndrome 47 0.038
161
ASP007 Aspiration Pneumonia 47 0.038
162
HRT007 Heart Cancer 46 0.038
163
GLC036 Glucagonoma 46 0.038
164
BLD053 Blood Platelet Disease 46 0.038
165
CHR563 Chronic Eosinophilic Leukemia 46 0.038
166
P PSD015 Pseudohypoparathyroidism 46 0.038
167
DFN245 Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct 46 0.038
168
c THR103 Thrombocytopenia, Congenital Amegakaryocytic 45 0.038
169
ECT078 Ectodermal Dysplasia 2, Clouston Type 45 0.038
170
P MTH007 Methemoglobinemia 45 0.038
171
RFR010 Refractory Anemia 45 0.038
172
P LYD001 Leydig Cell Tumor 44 0.038
173
VST004 Vestibular Disease 44 0.038
174
P RTN014 Retinal Artery Occlusion 44 0.038
175
CRT015 Carotid Artery Occlusion 43 0.038
176
c ACH035 Achondrogenesis Ib 43 0.038
177
LKC003 Leukocyte Disease 43 0.038
178
FCT005 Factor Xiii Deficiency 43 0.038
179
P MGS004 Meige Syndrome 43 0.038
180
CHR286 Chronic Neutrophilic Leukemia 43 0.038
181
P SPN042 Spinal Cord Ependymoma 43 0.038
182
MLT001 Multiple Chemical Sensitivity 43 0.038
183
EWN002 Ewing's Family of Tumors 43 0.038
184
c NNS007 Nonsyndromic Deafness 42 0.038
185
c ACQ014 Acquired Hemophilia 42 0.038
186
DDN006 Duodenitis 42 0.038
187
c DFN141 Deafness, Autosomal Recessive 12 42 0.038
188
HPT020 Hepatic Vascular Disease 42 0.038
189
AGG002 Aggressive Systemic Mastocytosis 42 0.038
190
P BLD051 Blood Coagulation Disease 42 0.038
191
CRB138 Core Binding Factor Acute Myeloid Leukemia 42 0.038
192
CHN010 Chondroma 42 0.038
193
IND002 Indolent Systemic Mastocytosis 41 0.038
194
MDL009 Medullary Sponge Kidney 41 0.038
195
VHW001 Vohwinkel Syndrome 41 0.038
196
SRC002 Sarcomatoid Renal Cell Carcinoma 41 0.038
197
PHC013 Phaeochromocytoma 41 0.038
198
ANM001 Anemia of Prematurity 41 0.038
199
NRN002 Neuronitis 41 0.038
200
CRC014 Carcinoid Tumors, Intestinal 40 0.038
201
c ACQ042 Acquired Hemophilia a 40 0.038
202
c DFN097 Deafness, Autosomal Recessive 1a 40 0.038
203
ADT003 Auditory System Disease 40 0.038
204
FBR002 Fibrosarcoma of Bone 40 0.038
205
P PRG017 Paraganglioma and Gastric Stromal Sarcoma 40 0.038
206
MST001 Mast-Cell Sarcoma 40 0.038
207
P HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 40 0.038
208
BRT001 Bart-Pumphrey Syndrome 40 0.038
209
MST004 Mast Cell Neoplasm 40 0.038
210
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 39 0.038
211
c CTR103 Cataract 4, Multiple Types 39 0.038
212
CRN055 Carney Triad 39 0.038
213
MDN005 Mednik Syndrome 39 0.038
214
c DFN251 Deafness, Autosomal Dominant 11 38 0.038
215
c PRM149 Primary Hypereosinophilic Syndrome 38 0.038
216
ACT113 Acute Myeloblastic Leukemia with Maturation 37 0.038
217
RTN013 Retinal Hemangioblastoma 37 0.038
218
CYC007 Cyclic Thrombocytopenia 37 0.038
219
CNG069 Congenital Cytomegalovirus 36 0.038
220
P ADT004 Auditory Neuropathy 36 0.038
221
TTR016 Tetra-Amelia Syndrome 36 0.038
222
P 8P1002 8p11 Myeloproliferative Syndrome 36 0.038
223
ADR014 Adrenal Medulla Cancer 36 0.038
224
c DFN143 Deafness, Autosomal Recessive 16 36 0.038
225
INT078 Intracranial Thrombosis 36 0.038
226
ALR002 Al-Raqad Syndrome 36 0.038
227
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 36 0.038
228
EXT054 Extra-Adrenal Pheochromocytoma 35 0.038
229
c DFN137 Deafness, Autosomal Dominant 13 35 0.038
230
ATS009 Autosomal Genetic Disease 35 0.038
231
PNC053 Pancreatic Islet Cell Tumors 35 0.038
232
ADP007 Adie Pupil 34 0.038
233
c DFN093 Deafness, Autosomal Recessive 23 34 0.038
234
FMR011 Fumarate Hydratase Deficiency 34 0.038
235
TRN030 Transient Erythroblastopenia of Childhood 34 0.038
236
BRS032 Breast Papillary Carcinoma 34 0.038
237
c DFN103 Deafness, Autosomal Recessive 1b 34 0.038
238
c GLL024 Gallbladder Disease 1 34 0.038
239
DDN005 Duodenal Somatostatinoma 34 0.038
240
FLC001 Folic Acid Deficiency Anemia 34 0.038
241
MYL015 Myeloproliferative Disorder with Eosinophilia 34 0.038
242
FML029 Familial Renal Papillary Carcinoma 34 0.038
243
c RNL047 Renal Tubular Acidosis, Distal, Autosomal Recessive 34 0.038
244
HDG001 Hodgkin's Lymphoma, Nodular Sclerosis 34 0.038
245
c DFN133 Deafness, Autosomal Recessive 9 34 0.038
246
FNT004 Fainting 33 0.038
247
ADR040 Adrenal Gland Pheochromocytoma 33 0.038
248
FCT016 Factor V and Factor Viii, Combined Deficiency of 33 0.038
249
c DFN128 Deafness, Autosomal Dominant 36 32 0.038
250
INT104 Intravascular Papillary Endothelial Hyperplasia 32 0.038
251
c DYS174 Dyskeratosis Congenita, Autosomal Dominant 6 32 0.038
252
PNC018 Pancreatic Serous Cystadenoma 32 0.038
253
PRS123 Persistent Generalized Lymphadenopathy 31 0.038
254
c ATS336 Autosomal Recessive Nonsyndromic Deafness 3 31 0.038
255
EPT008 Epithelioid Malignant Peripheral Nerve Sheath Tumor 30 0.038
256
c HRD020 Hereditary Renal Cell Carcinoma 30 0.038
257
c DFN151 Deafness, Autosomal Dominant 24 30 0.038
258
c ACQ010 Acquired Polycythemia 30 0.038
259
CRN273 Corneal Dystrophy, Subepithelial Mucinous 30 0.038
260
CMB005 Combined Factor V and Viii Deficiency 30 0.038
261
c DFN183 Deafness, Autosomal Recessive 83 30 0.038
262
c DFN184 Deafness, Autosomal Recessive 85 30 0.038
263
MYL059 Myeloid and Lymphoid Neoplasms with Eosinophilia and Abnormalities of Pdgfra, Pdgfrb, and Fgfr1 29 0.038
264
DFN038 Dfnb1 29 0.038
265
c ACT219 Acute Myeloid Leukemia, Flt3-Related 29 0.038
266
P RNL045 Renal Tubular Acidosis, Distal 29 0.038
267
PHY001 Physiological Polycythemia 28 0.038
268
c ACT194 Acute Myeloid Leukemia with T(8;21)(q22;q22) Translocation 28 0.038
269
c DFN178 Deafness, Autosomal Recessive 59 28 0.038
270
SQM005 Squamous Papillomatosis 28 0.038
271
NNS014 Nonsyndromic Hearing Loss and Deafness 28 0.038
272
c ATS342 Autosomal Dominant Nonsyndromic Deafness 6 28 0.038
273
MTN001 Metanephric Adenoma 28 0.038
274
c ADT007 Auditory Neuropathy, Autosomal Dominant, 1 28 0.038
275
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 26 0.038
276
DFN003 Deafness and Hereditary Hearing Loss 26 0.038
277
LCT003 Lactocele 26 0.038
278
c DFN168 Deafness, Autosomal Recessive 26 26 0.038
279
SMH001 Sm-Ahnmd 26 0.038
280
MXD003 Mixed Lacrimal Gland Cancer 26 0.038
281
MCR014 Microcystic Adenoma 25 0.038
282
NRL008 Neural Crest Tumor 25 0.038
283
PSD026 Pseudoainhum 24 0.038
284
ATS252 Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb 24 0.038
285
P CRN178 Coronary Heart Disease 6 21 0.038
286
DPL001 Deep Leiomyoma 21 0.038
287
RTC007 Reticular Perineurioma 20 0.038
288
CTR009 Cataract Congenital Dominant Non Nuclear 20 0.038
289
c CRN173 Coronary Heart Disease 8 18 0.038
290
HYP489 Hypotrichosis-Deafness Syndrome 18 0.038
291
NNS009 Nonsyndromic Hearing Loss and Deafness, Dfnb1 17 0.038
292
DFN042 Dfna 3 Nonsyndromic Hearing Loss and Deafness 17 0.038
293
DYS008 Dyshormonogenic Goiter 17 0.038
294
AND005 Androgen Insensitivity Syndrome, Mild 16 0.038
295
PND003 Pendred Syndrome/dfnb4 15 0.038
296
DFN063 Dfnb 1 Nonsyndromic Hearing Loss and Deafness 15 0.038
297
AQG001 Aquagenic Pruritus 15 0.038
298
NNS008 Nonsyndromic Hearing Loss and Deafness, Dfna3 13 0.038
299
ATY026 Atypical Meigs Syndrome 9 0.038
Content
Loading form....