Search results for "erythrocytosis"

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

122 hits were found for 'erythrocytosis'

# Family MCID Name MIFTS Score
1
ERY045 Erythrocytosis, Somatic 36 7.016
2
c PRM012 Primary Polycythemia 56 6.545
3
P ERY048 Erythrocytosis, Familial, 2 44 5.772
4
c ERY032 Erythrocytosis, Familial, 4 17 4.978
5
c ERY031 Erythrocytosis, Familial, 3 16 4.978
6
ERY044 Erythrocytosis Due to Bisphosphoglycerate Mutase Deficiency 19 4.072
7
TMP008 Tempi Syndrome 21 2.918
8
ATS075 Autosomal Recessive Secondary Polycythemia Not Associated with Vhl Gene 6 2.830
9
CHV001 Chuvash Erythrocytosis 11 2.108
10
PLY125 Polycythemia Vera, Somatic 64 2.045
11
c ATS209 Autosomal Dominant Secondary Polycythemia 17 2.045
12
ERY007 Erythropoietin Polycythemia 17 2.045
13
STR007 Stress Polycythemia 20 2.001
14
PSD044 Pseudopolycythaemia 12 2.001
15
MLT106 Multiple Paragangliomas Associated with Polycythemia 9 2.001
16
P PLY018 Polycythemia 57 0.219
17
HMN009 Hemangioblastoma 51 0.150
18
c CHR546 Chronic Mountain Sickness 45 0.141
19
MYM001 Myoma 54 0.130
20
P HPT021 Hepatitis 77 0.119
21
THR004 Thrombocytosis 56 0.119
22
ADN018 Adenoma 62 0.106
23
P THL005 Thalassemia 62 0.106
24
HYP266 Hypoxia 60 0.106
25
P PRG013 Paraganglioma 54 0.106
26
RNL007 Renal Tubular Acidosis 50 0.106
27
NPH003 Nephrocalcinosis 47 0.106
28
HPT023 Hepatocellular Carcinoma 90 0.092
29
P PHC003 Pheochromocytoma 71 0.092
30
P ACT105 Acute Mountain Sickness 58 0.092
31
HYP043 Hyperandrogenism 51 0.092
32
P LKM002 Leukemia 70 0.075
33
c CNG401 Congenital Heart Disease 70 0.075
34
P HMC003 Hemochromatosis 68 0.075
35
HYP056 Hypoglycemia 60 0.075
36
LMY002 Leiomyoma 56 0.075
37
P HYP014 Hyperuricemia 53 0.075
38
P RNL017 Renal Oncocytoma 50 0.075
39
CRB009 Cerebritis 48 0.075
40
GLM011 Glomerulosclerosis 46 0.075
41
c SPR094 Sporadic Pheochromocytoma 38 0.075
42
HPT074 Hepatic Adenoma, Somatic 36 0.075
43
HRS011 Horseshoe Kidney 29 0.075
44
P RNL014 Renal Cell Carcinoma 80 0.053
45
c MLT019 Multiple Myeloma 77 0.053
46
INS024 Insulin-Like Growth Factor I 76 0.053
47
GST019 Gastrointestinal Stromal Tumor 74 0.053
48
P APL001 Aplastic Anemia 73 0.053
49
c HPT001 Hepatitis C 72 0.053
50
CNG034 Congestive Heart Failure 72 0.053
51
P NRB001 Neuroblastoma 72 0.053
52
P PLY014 Polycystic Kidney Disease 70 0.053
53
P ADN016 Adenocarcinoma 69 0.053
54
VNH007 Von Hippel-Lindau Syndrome 69 0.053
55
P MYL005 Myelofibrosis 68 0.053
56
P AMY004 Amyloidosis 68 0.053
57
P RSP003 Respiratory Failure 68 0.053
58
P HRT032 Heart Disease 68 0.053
59
P PNM007 Pneumonia 68 0.053
60
P KDN017 Kidney Cancer 67 0.053
61
LVR012 Liver Cirrhosis 66 0.053
62
P ESS003 Essential Thrombocythemia 66 0.053
63
P RCK004 Rickets 62 0.053
64
RSP006 Respiratory System Disease 62 0.053
65
P INT001 Intrahepatic Cholestasis 61 0.053
66
DFC004 Deficiency Anemia 60 0.053
67
c ACT073 Acute Leukemia 60 0.053
68
P KDN018 Kidney Disease 60 0.053
69
P HYP020 Hyperprolactinemia 60 0.053
70
P HML002 Hemolytic Anemia 59 0.053
71
UTR039 Uterine Fibroid 58 0.053
72
END030 End Stage Renal Failure 58 0.053
73
P BRS044 Breast Adenocarcinoma 58 0.053
74
P MYL007 Myeloma 58 0.053
75
PLM033 Pulmonary Embolism 57 0.053
76
CHL068 Cholestasis 57 0.053
77
c ALM001 Al Amyloidosis 56 0.053
78
P CLR030 Clear Cell Renal Cell Carcinoma 56 0.053
79
P HYP076 Hyperthyroidism 56 0.053
80
c RNL003 Renal Clear Cell Carcinoma 56 0.053
81
PTT006 Pituitary Adenoma 55 0.053
82
HPT022 Hepatoblastoma 55 0.053
83
CHL067 Cholecystitis 53 0.053
84
P FNC004 Fanconi Syndrome 53 0.053
85
ACT098 Acute Erythroid Leukemia 52 0.053
86
P HYP613 Hypophosphatemic Rickets 51 0.053
87
P HYD002 Hydronephrosis 50 0.053
88
P MGS004 Meige Syndrome 50 0.053
89
SMT003 Somatostatinoma 50 0.053
90
PLC003 Placental Site Trophoblastic Tumor 50 0.053
91
PHC013 Phaeochromocytoma 49 0.053
92
P MTH007 Methemoglobinemia 49 0.053
93
THR013 Thoracic Outlet Syndrome 49 0.053
94
P PSD015 Pseudohypoparathyroidism 49 0.053
95
DDN006 Duodenitis 47 0.053
96
P LYD001 Leydig Cell Tumor 47 0.053
97
CHL004 Cholelithiasis 46 0.053
98
ANM001 Anemia of Prematurity 46 0.053
99
MLT001 Multiple Chemical Sensitivity 46 0.053
100
SPL018 Splenomegaly 46 0.053
101
ASP007 Aspiration Pneumonia 45 0.053
102
HPT002 Hepatic Vein Thrombosis 45 0.053
103
P ART084 Arteriovenous Fistula 44 0.053
104
c GLL024 Gallbladder Disease 1 42 0.053
105
FNT004 Fainting 41 0.053
106
NRN002 Neuronitis 41 0.053
107
FMR011 Fumarate Hydratase Deficiency 41 0.053
108
RTN013 Retinal Hemangioblastoma 40 0.053
109
BLD054 Blood Protein Disease 40 0.053
110
NNT011 Neonatal Anemia 38 0.053
111
TTR016 Tetra-Amelia Syndrome 36 0.053
112
c ACQ010 Acquired Polycythemia 35 0.053
113
PHY001 Physiological Polycythemia 33 0.053
114
DDN005 Duodenal Somatostatinoma 33 0.053
115
ALR002 Al-Raqad Syndrome 27 0.053
116
MTN001 Metanephric Adenoma 25 0.053
117
P CRN178 Coronary Heart Disease 6 22 0.053
118
c CRN173 Coronary Heart Disease 8 21 0.053
119
AND005 Androgen Insensitivity Syndrome, Mild 21 0.053
120
AQG001 Aquagenic Pruritus 20 0.053
121
c ATS229 Autosomal Recessive Lymphoproliferative Disease 19 0.053
122
ATY026 Atypical Meigs Syndrome 10 0.053