Search results for erythrocytosis

146 hits were found for erythrocytosis

# Family MCID Name MIFTS Score
1
P ERY058 Erythrocytosis, Familial, 1 55 9.345
2
c ERY048 Erythrocytosis, Familial, 2 48 6.470
3
c PRM012 Primary Polycythemia 53 5.615
4
c ERY031 Erythrocytosis, Familial, 3 15 4.600
5
c ERY032 Erythrocytosis, Familial, 4 14 4.566
6
BSP004 Bisphosphoglycerate Mutase Deficiency 20 3.518
7
TMP008 Tempi Syndrome 25 2.933
8
ATS075 Autosomal Recessive Secondary Polycythemia Not Associated with Vhl Gene 6 2.851
9
PLY001 Polycythemia Vera 75 2.327
10
ERY007 Erythropoietin Polycythemia 14 2.215
11
c ATS209 Autosomal Dominant Secondary Polycythemia 16 2.057
12
STR007 Stress Polycythemia 16 2.016
13
PSD044 Pseudopolycythaemia 11 2.016
14
MLT106 Multiple Paragangliomas Associated with Polycythemia 9 2.016
15
P PLY018 Polycythemia 60 0.223
16
HMN009 Hemangioblastoma 56 0.141
17
c CHR546 Chronic Mountain Sickness 45 0.132
18
MYM001 Myoma 56 0.122
19
THR004 Thrombocytosis 55 0.122
20
P HPT021 Hepatitis 75 0.111
21
VNH007 Von Hippel-Lindau Syndrome 72 0.111
22
THR024 Thrombosis 61 0.111
23
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.111
24
P HPT023 Hepatocellular Carcinoma 94 0.100
25
P ANR048 Aniridia 1 68 0.100
26
P THL005 Thalassemia 65 0.100
27
ADN018 Adenoma 63 0.100
28
HYP266 Hypoxia 61 0.100
29
P PRG013 Paraganglioma 57 0.100
30
P RNL007 Renal Tubular Acidosis 51 0.100
31
NPH003 Nephrocalcinosis 49 0.100
32
ANR038 Anorexia Nervosa 1 21 0.100
33
BLD137 Blood Group--Ahonen 17 0.100
34
P PHC003 Pheochromocytoma 72 0.086
35
P ACT105 Acute Mountain Sickness 58 0.086
36
HYP043 Hyperandrogenism 50 0.086
37
P RNL045 Renal Tubular Acidosis, Distal 42 0.086
38
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.086
39
c BLD140 Blood Group, I System 37 0.086
40
P MYL005 Myelofibrosis 75 0.070
41
P LKM002 Leukemia 75 0.070
42
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.070
43
APL001 Aplastic Anemia 74 0.070
44
c HMC039 Hemochromatosis, Type 1 71 0.070
45
P ESS003 Essential Thrombocythemia 71 0.070
46
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.070
47
HYP056 Hypoglycemia 62 0.070
48
LMY014 Leiomyoma, Uterine 61 0.070
49
LMY002 Leiomyoma 58 0.070
50
P HYP014 Hyperuricemia 54 0.070
51
ACT098 Acute Erythroid Leukemia 52 0.070
52
HPT082 Hepatic Adenomas, Familial 52 0.070
53
P RNL017 Renal Oncocytoma 49 0.070
54
ONC007 Oncocytoma 48 0.070
55
ANM001 Anemia of Prematurity 43 0.070
56
CRB009 Cerebritis 41 0.070
57
c SPR094 Sporadic Pheochromocytoma 38 0.070
58
NNT011 Neonatal Anemia 35 0.070
59
HRS011 Horseshoe Kidney 35 0.070
60
c ACQ010 Acquired Polycythemia 33 0.070
61
ALR002 Al-Raqad Syndrome 30 0.070
62
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.070
63
HMG031 Hemoglobin, High Altitude Adaptation 11 0.070
64
MYL069 Myeloma, Multiple 86 0.050
65
STR067 Stroke, Ischemic 84 0.050
66
INS024 Insulin-Like Growth Factor I 83 0.050
67
c LKM063 Leukemia, Chronic Myeloid 80 0.050
68
P HRT032 Heart Disease 80 0.050
69
ALP046 Alport Syndrome, X-Linked 74 0.050
70
GST019 Gastrointestinal Stromal Tumor 74 0.050
71
CNG034 Congestive Heart Failure 74 0.050
72
c HPT001 Hepatitis C 73 0.050
73
P NRB001 Neuroblastoma 73 0.050
74
LVR012 Liver Cirrhosis 73 0.050
75
P ADN016 Adenocarcinoma 71 0.050
76
P PNM007 Pneumonia 70 0.050
77
c MNN043 Meningioma, Familial 69 0.050
78
P KDN018 Kidney Disease 69 0.050
79
P AMY004 Amyloidosis 69 0.050
80
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.050
81
AGN016 Aging 65 0.050
82
MYL031 Myeloproliferative Neoplasm 64 0.050
83
HYP020 Hyperprolactinemia 64 0.050
84
RSP006 Respiratory System Disease 63 0.050
85
MGK001 Megakaryocytic Leukemia 63 0.050
86
RCK004 Rickets 63 0.050
87
PLM033 Pulmonary Embolism 62 0.050
88
DFC004 Deficiency Anemia 62 0.050
89
P INT001 Intrahepatic Cholestasis 62 0.050
90
c ACT073 Acute Leukemia 61 0.050
91
CHL068 Cholestasis 60 0.050
92
P PLY014 Polycystic Kidney Disease 60 0.050
93
c ALP101 Alpha-Thalassemia 60 0.050
94
CHR177 Chromophobe Renal Cell Carcinoma 59 0.050
95
END030 End Stage Renal Failure 59 0.050
96
ALL026 Allergic Hypersensitivity Disease 59 0.050
97
c FCL025 Focal Segmental Glomerulosclerosis 1 59 0.050
98
P BRS044 Breast Adenocarcinoma 58 0.050
99
P PTT006 Pituitary Adenoma 57 0.050
100
c ALM001 Al Amyloidosis 56 0.050
101
P HYP076 Hyperthyroidism 56 0.050
102
HPT022 Hepatoblastoma 55 0.050
103
HDC001 Headache 55 0.050
104
c LYM130 Lymphedema, Hereditary, Ii 55 0.050
105
P FNC004 Fanconi Syndrome 54 0.050
106
SMT003 Somatostatinoma 54 0.050
107
HYP080 Hypogonadism 54 0.050
108
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.050
109
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 53 0.050
110
BNM001 Bone Marrow Cancer 52 0.050
111
c AMG001 Amegakaryocytic Thrombocytopenia, Congenital 51 0.050
112
P PSD015 Pseudohypoparathyroidism 50 0.050
113
HMS001 Hemosiderosis 50 0.050
114
HYD002 Hydronephrosis 49 0.050
115
HYP063 Hypersplenism 49 0.050
116
ASP007 Aspiration Pneumonia 49 0.050
117
EWN002 Ewing's Family of Tumors 49 0.050
118
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.050
119
RFR010 Refractory Anemia 48 0.050
120
P LYD001 Leydig Cell Tumor 47 0.050
121
P MTH007 Methemoglobinemia 46 0.050
122
PLC003 Placental Site Trophoblastic Tumor 46 0.050
123
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 46 0.050
124
ISL114 Isolated Growth Hormone Deficiency, Type Ii 46 0.050
125
DDN006 Duodenitis 46 0.050
126
END072 Endotheliitis 46 0.050
127
SPL018 Splenomegaly 45 0.050
128
c WLM011 Wilms Tumor 6 44 0.050
129
NRN002 Neuronitis 43 0.050
130
SPL012 Splenic Disease 42 0.050
131
ADP007 Adie Pupil 41 0.050
132
TTR025 Tetraamelia Syndrome, Autosomal Recessive 40 0.050
133
RTN013 Retinal Hemangioblastoma 38 0.050
134
c THR090 Thrombocythemia 1 37 0.050
135
FNT004 Fainting 36 0.050
136
JK3001 Jak3-Deficient Severe Combined Immunodeficiency 35 0.050
137
FMR011 Fumarate Hydratase Deficiency 32 0.050
138
CLL007 Cellular Congenital Mesoblastic Nephroma 31 0.050
139
MYL059 Myeloid and Lymphoid Neoplasms with Eosinophilia and Abnormalities of Pdgfra, Pdgfrb, and Fgfr1 31 0.050
140
MTN001 Metanephric Adenoma 31 0.050
141
DDN005 Duodenal Somatostatinoma 30 0.050
142
FLC001 Folic Acid Deficiency Anemia 30 0.050
143
BCL001 B Cell Linker Protein Deficiency 29 0.050
144
BLD163 Blood Group, Dombrock System 23 0.050
145
AQG001 Aquagenic Pruritus 16 0.050
146
ATY026 Atypical Meigs Syndrome 10 0.050
Content
Loading form....