Search results for "erythrocytosis"

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

112 hits were found for 'erythrocytosis'

# Family MCID Name MIFTS Score
1
ERY045 Erythrocytosis, Somatic 35 8.923
2
P ERY048 Erythrocytosis, Familial, 2 42 6.463
3
c PRM012 Primary Polycythemia 51 5.575
4
c ERY032 Erythrocytosis, Familial, 4 17 5.024
5
c ERY031 Erythrocytosis, Familial, 3 17 5.024
6
ERY044 Erythrocytosis Due to Bisphosphoglycerate Mutase Deficiency 19 4.109
7
TMP008 Tempi Syndrome 21 2.919
8
ATS075 Autosomal Recessive Secondary Polycythemia Not Associated with Vhl Gene 5 2.856
9
c ATS209 Autosomal Dominant Secondary Polycythemia 16 2.064
10
ERY007 Erythropoietin Polycythemia 15 2.064
11
PLY125 Polycythemia Vera, Somatic 63 2.019
12
STR007 Stress Polycythemia 16 2.019
13
PSD044 Pseudopolycythaemia 9 2.019
14
MLT106 Multiple Paragangliomas Associated with Polycythemia 7 2.019
15
P PLY018 Polycythemia 57 0.230
16
HMN009 Hemangioblastoma 45 0.153
17
c CHR546 Chronic Mountain Sickness 42 0.143
18
MYM001 Myoma 51 0.133
19
P HPT021 Hepatitis 70 0.121
20
THR004 Thrombocytosis 55 0.121
21
HPT023 Hepatocellular Carcinoma 91 0.108
22
P THL005 Thalassemia 61 0.108
23
ADN018 Adenoma 59 0.108
24
HYP266 Hypoxia 55 0.108
25
RNL007 Renal Tubular Acidosis 50 0.108
26
NPH003 Nephrocalcinosis 46 0.108
27
P PHC003 Pheochromocytoma 71 0.094
28
P ACT105 Acute Mountain Sickness 53 0.094
29
HYP043 Hyperandrogenism 48 0.094
30
P HRT032 Heart Disease 76 0.077
31
P HMC003 Hemochromatosis 72 0.077
32
P LKM002 Leukemia 70 0.077
33
HYP056 Hypoglycemia 61 0.077
34
HPT074 Hepatic Adenoma, Somatic 51 0.077
35
P HYP014 Hyperuricemia 50 0.077
36
P RNL017 Renal Oncocytoma 46 0.077
37
GLM011 Glomerulosclerosis 44 0.077
38
LMY002 Leiomyoma 42 0.077
39
CRB009 Cerebritis 38 0.077
40
c SPR094 Sporadic Pheochromocytoma 35 0.077
41
HRS011 Horseshoe Kidney 35 0.077
42
ADP007 Adie Pupil 34 0.077
43
HNM002 Hinman Syndrome 25 0.077
44
P RNL014 Renal Cell Carcinoma 81 0.054
45
P MLT019 Multiple Myeloma 80 0.054
46
STR067 Stroke, Ischemic 77 0.054
47
INS024 Insulin-Like Growth Factor I 74 0.054
48
P APL001 Aplastic Anemia 73 0.054
49
GST019 Gastrointestinal Stromal Tumor 72 0.054
50
CNG034 Congestive Heart Failure 71 0.054
51
P RSP003 Respiratory Failure 70 0.054
52
P ADN016 Adenocarcinoma 69 0.054
53
VNH007 Von Hippel-Lindau Syndrome 69 0.054
54
P NRB001 Neuroblastoma 69 0.054
55
c HPT001 Hepatitis C 68 0.054
56
P ESS003 Essential Thrombocythemia 68 0.054
57
P MYL005 Myelofibrosis 67 0.054
58
LVR012 Liver Cirrhosis 67 0.054
59
P PNM007 Pneumonia 66 0.054
60
P AMY004 Amyloidosis 64 0.054
61
RSP006 Respiratory System Disease 62 0.054
62
c ACT073 Acute Leukemia 62 0.054
63
P HML002 Hemolytic Anemia 60 0.054
64
P BRS044 Breast Adenocarcinoma 60 0.054
65
P RCK004 Rickets 59 0.054
66
PLM033 Pulmonary Embolism 59 0.054
67
CHL068 Cholestasis 58 0.054
68
HYP020 Hyperprolactinemia 57 0.054
69
P INT001 Intrahepatic Cholestasis 57 0.054
70
CHL067 Cholecystitis 56 0.054
71
P HYP076 Hyperthyroidism 56 0.054
72
PTT006 Pituitary Adenoma 55 0.054
73
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.054
74
HPT022 Hepatoblastoma 53 0.054
75
END030 End Stage Renal Failure 52 0.054
76
CLR030 Clear Cell Renal Cell Carcinoma 51 0.054
77
P HYP613 Hypophosphatemic Rickets 51 0.054
78
THR013 Thoracic Outlet Syndrome 49 0.054
79
ACT098 Acute Erythroid Leukemia 48 0.054
80
CHL004 Cholelithiasis 48 0.054
81
HYD002 Hydronephrosis 47 0.054
82
PLC003 Placental Site Trophoblastic Tumor 47 0.054
83
ASP007 Aspiration Pneumonia 46 0.054
84
EWN002 Ewing's Family of Tumors 45 0.054
85
P MGS004 Meige Syndrome 45 0.054
86
P MTH007 Methemoglobinemia 45 0.054
87
P PSD015 Pseudohypoparathyroidism 44 0.054
88
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.054
89
DDN006 Duodenitis 44 0.054
90
c ALM001 Al Amyloidosis 44 0.054
91
SPL018 Splenomegaly 44 0.054
92
P LYD001 Leydig Cell Tumor 44 0.054
93
MLT001 Multiple Chemical Sensitivity 43 0.054
94
ANM001 Anemia of Prematurity 43 0.054
95
SMT003 Somatostatinoma 42 0.054
96
NRN002 Neuronitis 42 0.054
97
c GLL024 Gallbladder Disease 1 38 0.054
98
RTN013 Retinal Hemangioblastoma 37 0.054
99
ALR002 Al-Raqad Syndrome 36 0.054
100
TTR016 Tetra-Amelia Syndrome 36 0.054
101
NNT011 Neonatal Anemia 34 0.054
102
FMR011 Fumarate Hydratase Deficiency 34 0.054
103
FNT004 Fainting 33 0.054
104
DDN005 Duodenal Somatostatinoma 33 0.054
105
PHY001 Physiological Polycythemia 31 0.054
106
c ACQ010 Acquired Polycythemia 31 0.054
107
MTN001 Metanephric Adenoma 27 0.054
108
P CRN178 Coronary Heart Disease 6 24 0.054
109
c CRN173 Coronary Heart Disease 8 20 0.054
110
AQG001 Aquagenic Pruritus 17 0.054
111
AND005 Androgen Insensitivity Syndrome, Mild 16 0.054
112
ATY026 Atypical Meigs Syndrome 9 0.054