Search results for "erythrocytosis"

The MalaCard for "erythrocytosis" has been retired.
Searching MalaCards for entries containing "erythrocytosis"

116 hits were found for 'erythrocytosis'

# Family MCID Name MIFTS Score
1
ERY045 Erythrocytosis, Somatic 36 8.224
2
P ERY048 Erythrocytosis, Familial, 2 42 6.177
3
c PRM012 Primary Polycythemia 48 5.614
4
c ERY031 Erythrocytosis, Familial, 3 17 5.038
5
c ERY032 Erythrocytosis, Familial, 4 17 5.038
6
ERY044 Erythrocytosis Due to Bisphosphoglycerate Mutase Deficiency 19 4.107
7
TMP008 Tempi Syndrome 20 2.943
8
ATS075 Autosomal Recessive Secondary Polycythemia Not Associated with Vhl Gene 5 2.855
9
PLY125 Polycythemia Vera, Somatic 63 2.097
10
c ATS209 Autosomal Dominant Secondary Polycythemia 16 2.097
11
ERY007 Erythropoietin Polycythemia 14 2.063
12
STR007 Stress Polycythemia 17 2.019
13
PSD044 Pseudopolycythaemia 10 2.019
14
MLT106 Multiple Paragangliomas Associated with Polycythemia 7 2.019
15
P PLY018 Polycythemia 58 0.233
16
HMN009 Hemangioblastoma 45 0.161
17
c CHR546 Chronic Mountain Sickness 42 0.142
18
MYM001 Myoma 51 0.131
19
P PRG013 Paraganglioma 54 0.131
20
P HPT021 Hepatitis 74 0.120
21
THR004 Thrombocytosis 55 0.120
22
HYP266 Hypoxia 55 0.120
23
P THL005 Thalassemia 61 0.107
24
HPT074 Hepatic Adenoma, Somatic 35 0.107
25
RNL007 Renal Tubular Acidosis 50 0.107
26
P ACT105 Acute Mountain Sickness 55 0.107
27
NPH003 Nephrocalcinosis 47 0.107
28
ADN018 Adenoma 59 0.107
29
HPT023 Hepatocellular Carcinoma 90 0.093
30
P PHC003 Pheochromocytoma 72 0.093
31
P LKM002 Leukemia 70 0.093
32
HYP043 Hyperandrogenism 46 0.093
33
c SPR094 Sporadic Pheochromocytoma 34 0.093
34
P HMC003 Hemochromatosis 71 0.076
35
VNH007 Von Hippel-Lindau Syndrome 69 0.076
36
c CNG401 Congenital Heart Disease 67 0.076
37
CHL067 Cholecystitis 57 0.076
38
THR013 Thoracic Outlet Syndrome 48 0.076
39
P HML002 Hemolytic Anemia 60 0.076
40
HYP056 Hypoglycemia 60 0.076
41
HMR001 Hemorrhagic Thrombocythemia 47 0.076
42
P HYP014 Hyperuricemia 49 0.076
43
LMY002 Leiomyoma 56 0.076
44
c RNL003 Renal Clear Cell Carcinoma 49 0.076
45
ALR002 Al-Raqad Syndrome 36 0.076
46
P RNL017 Renal Oncocytoma 48 0.076
47
SPL018 Splenomegaly 45 0.076
48
CLR030 Clear Cell Renal Cell Carcinoma 52 0.076
49
c ACQ010 Acquired Polycythemia 31 0.076
50
CHL004 Cholelithiasis 48 0.076
51
EWN002 Ewing's Family of Tumors 45 0.076
52
HRS011 Horseshoe Kidney 34 0.076
53
ANM001 Anemia of Prematurity 44 0.076
54
NNT011 Neonatal Anemia 34 0.076
55
FMR011 Fumarate Hydratase Deficiency 34 0.076
56
GLM011 Glomerulosclerosis 41 0.076
57
CRB009 Cerebritis 36 0.076
58
RTN013 Retinal Hemangioblastoma 37 0.076
59
c MLT019 Multiple Myeloma 77 0.054
60
P RNL014 Renal Cell Carcinoma 80 0.054
61
P NRB001 Neuroblastoma 70 0.054
62
P RSP003 Respiratory Failure 68 0.054
63
P APL001 Aplastic Anemia 74 0.054
64
CNG034 Congestive Heart Failure 72 0.054
65
P ESS003 Essential Thrombocythemia 66 0.054
66
GST019 Gastrointestinal Stromal Tumor 73 0.054
67
P KDN018 Kidney Disease 64 0.054
68
PLM033 Pulmonary Embolism 59 0.054
69
RSP006 Respiratory System Disease 61 0.054
70
P MYL005 Myelofibrosis 67 0.054
71
INS024 Insulin-Like Growth Factor I 75 0.054
72
P RCK004 Rickets 59 0.054
73
c HPT001 Hepatitis C 68 0.054
74
P INT001 Intrahepatic Cholestasis 58 0.054
75
P HYP613 Hypophosphatemic Rickets 50 0.054
76
LVR012 Liver Cirrhosis 71 0.054
77
HYP020 Hyperprolactinemia 58 0.054
78
P MGS004 Meige Syndrome 46 0.054
79
P HYP076 Hyperthyroidism 59 0.054
80
P PNM007 Pneumonia 67 0.054
81
UTR039 Uterine Fibroid 55 0.054
82
SMT003 Somatostatinoma 43 0.054
83
CHL068 Cholestasis 57 0.054
84
c ALM001 Al Amyloidosis 45 0.054
85
P ADN016 Adenocarcinoma 69 0.054
86
c ACT073 Acute Leukemia 61 0.054
87
P HRT032 Heart Disease 64 0.054
88
P PLY014 Polycystic Kidney Disease 60 0.054
89
P FNC004 Fanconi Syndrome 54 0.054
90
LPD004 Lipoid Nephrosis 49 0.054
91
END030 End Stage Renal Failure 53 0.054
92
HPT022 Hepatoblastoma 57 0.054
93
PLC003 Placental Site Trophoblastic Tumor 48 0.054
94
DDN006 Duodenitis 44 0.054
95
P CRN178 Coronary Heart Disease 6 22 0.054
96
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.054
97
P AMY004 Amyloidosis 63 0.054
98
P BRS044 Breast Adenocarcinoma 58 0.054
99
ASP007 Aspiration Pneumonia 46 0.054
100
PTT006 Pituitary Adenoma 54 0.054
101
HYD002 Hydronephrosis 48 0.054
102
MLT001 Multiple Chemical Sensitivity 43 0.054
103
P MTH007 Methemoglobinemia 44 0.054
104
P MYL007 Myeloma 52 0.054
105
AQG001 Aquagenic Pruritus 17 0.054
106
P PSD015 Pseudohypoparathyroidism 43 0.054
107
HPT002 Hepatic Vein Thrombosis 38 0.054
108
DDN005 Duodenal Somatostatinoma 34 0.054
109
MTN001 Metanephric Adenoma 28 0.054
110
c CRN173 Coronary Heart Disease 8 19 0.054
111
P LYD001 Leydig Cell Tumor 40 0.054
112
BLD054 Blood Protein Disease 38 0.054
113
NRN002 Neuronitis 40 0.054
114
ATY026 Atypical Meigs Syndrome 9 0.054
115
FNT004 Fainting 33 0.054
116
PHY001 Physiological Polycythemia 31 0.054