Search results for "erythrocytosis"

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

119 hits were found for 'erythrocytosis'

# Family MCID Name MIFTS Score
1
ERY045 Erythrocytosis, Somatic 41 6.497
2
c PRM012 Primary Polycythemia 47 5.966
3
PSD044 Pseudopolycythaemia 31 5.037
4
P ERY048 Erythrocytosis, Familial, 2 19 4.584
5
c ERY032 Erythrocytosis, Familial, 4 14 4.561
6
c ERY031 Erythrocytosis, Familial, 3 14 4.561
7
ERY044 Erythrocytosis Due to Bisphosphoglycerate Mutase Deficiency 16 3.561
8
TMP008 Tempi Syndrome 13 2.971
9
STR007 Stress Polycythemia 15 2.885
10
CHV001 Chuvash Erythrocytosis 10 2.885
11
ATS075 Autosomal Recessive Secondary Polycythemia Not Associated with Vhl Gene 7 2.885
12
c ATS209 Autosomal Dominant Secondary Polycythemia 16 2.040
13
MLT106 Multiple Paragangliomas Associated with Polycythemia 11 2.040
14
P PLY018 Polycythemia 59 0.217
15
PLY001 Polycythemia Vera 85 0.175
16
HMN009 Hemangioblastoma 54 0.139
17
MYM001 Myoma 53 0.129
18
HPT023 Hepatocellular Carcinoma 100 0.118
19
P HPT021 Hepatitis 63 0.118
20
THR004 Thrombocytosis 59 0.118
21
P THL005 Thalassemia 73 0.105
22
ADN018 Adenoma 64 0.105
23
RNL007 Renal Tubular Acidosis 56 0.105
24
P PRG013 Paraganglioma 54 0.105
25
NPH003 Nephrocalcinosis 48 0.105
26
CRB009 Cerebritis 37 0.105
27
VNH007 Von Hippel-Lindau Syndrome 74 0.091
28
ACN002 Acanthosis Nigricans 63 0.091
29
HYP266 Hypoxia 57 0.091
30
THR013 Thoracic Outlet Syndrome 52 0.091
31
HYP043 Hyperandrogenism 48 0.091
32
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 42 0.091
33
P ATX010 Ataxia Neuropathy Spectrum 29 0.091
34
P PHC003 Pheochromocytoma 88 0.075
35
P HMC003 Hemochromatosis 86 0.075
36
P MYL005 Myelofibrosis 78 0.075
37
P LKM002 Leukemia 76 0.075
38
P ESS003 Essential Thrombocythemia 75 0.075
39
LMY002 Leiomyoma 68 0.075
40
HYP056 Hypoglycemia 62 0.075
41
HDC001 Headache 57 0.075
42
P HYP014 Hyperuricemia 54 0.075
43
SCH016 Schimke Immunoosseous Dysplasia 53 0.075
44
SPL018 Splenomegaly 46 0.075
45
GLM011 Glomerulosclerosis 46 0.075
46
P TRC086 Trichohepatoenteric Syndrome 1 45 0.075
47
HRS011 Horseshoe Kidney 44 0.075
48
TTR016 Tetra-Amelia Syndrome 42 0.075
49
CRB085 Cerebral Hemorrhage 40 0.075
50
P MYC007 Myocardial Infarction 93 0.053
51
P APL001 Aplastic Anemia 86 0.053
52
c MLT019 Multiple Myeloma 85 0.053
53
GST019 Gastrointestinal Stromal Tumor 84 0.053
54
P RNL014 Renal Cell Carcinoma 83 0.053
55
c AMY091 Amyotrophic Lateral Sclerosis 1 81 0.053
56
CDS001 Cadasil 81 0.053
57
AND015 Androgen Insensitivity 78 0.053
58
P PNM007 Pneumonia 76 0.053
59
LVR012 Liver Cirrhosis 75 0.053
60
P AMY004 Amyloidosis 73 0.053
61
P NRB001 Neuroblastoma 72 0.053
62
P CNG401 Congenital Heart Disease 70 0.053
63
P HMN010 Hemangioma 69 0.053
64
STR067 Stroke, Ischemic 69 0.053
65
P RCK004 Rickets 67 0.053
66
CRB039 Cerebrovascular Disease 66 0.053
67
P HYP020 Hyperprolactinemia 66 0.053
68
PLM033 Pulmonary Embolism 66 0.053
69
INS024 Insulin-Like Growth Factor I 65 0.053
70
c HPT001 Hepatitis C 65 0.053
71
P HML002 Hemolytic Anemia 65 0.053
72
c ALM001 Al Amyloidosis 65 0.053
73
P KDN018 Kidney Disease 64 0.053
74
P INT001 Intrahepatic Cholestasis 63 0.053
75
ACT105 Acute Mountain Sickness 62 0.053
76
P HYP076 Hyperthyroidism 62 0.053
77
c HYP595 Hypertension, Essential 62 0.053
78
HPT022 Hepatoblastoma 61 0.053
79
P PLY014 Polycystic Kidney Disease 61 0.053
80
DFC004 Deficiency Anemia 61 0.053
81
PTT006 Pituitary Adenoma 60 0.053
82
CHL067 Cholecystitis 59 0.053
83
MYC002 Mycobacterium Avium Complex Disease 59 0.053
84
P MTH007 Methemoglobinemia 59 0.053
85
SMT003 Somatostatinoma 59 0.053
86
P MYL007 Myeloma 59 0.053
87
PLC003 Placental Site Trophoblastic Tumor 58 0.053
88
CHL068 Cholestasis 58 0.053
89
P ADN016 Adenocarcinoma 57 0.053
90
P AXN010 Axenfeld-Rieger Syndrome, Type 3 57 0.053
91
END030 End Stage Renal Failure 57 0.053
92
THY022 Thymic Carcinoma 57 0.053
93
DDN006 Duodenitis 55 0.053
94
P HYP613 Hypophosphatemic Rickets 55 0.053
95
c ACT073 Acute Leukemia 55 0.053
96
P PSD015 Pseudohypoparathyroidism 54 0.053
97
P HYD002 Hydronephrosis 52 0.053
98
P FNC004 Fanconi Syndrome 51 0.053
99
CYS016 Cystic Kidney 51 0.053
100
P LYD001 Leydig Cell Tumor 48 0.053
101
ASP007 Aspiration Pneumonia 47 0.053
102
CHL004 Cholelithiasis 47 0.053
103
HPT002 Hepatic Vein Thrombosis 46 0.053
104
P BRS044 Breast Adenocarcinoma 45 0.053
105
VRC005 Varicose Veins 45 0.053
106
NRN002 Neuronitis 42 0.053
107
MTN001 Metanephric Adenoma 41 0.053
108
P RNL017 Renal Oncocytoma 40 0.053
109
UTR039 Uterine Fibroid 39 0.053
110
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 39 0.053
111
FNT004 Fainting 38 0.053
112
ADS002 Adie Syndrome 34 0.053
113
SPR094 Sporadic Pheochromocytoma 32 0.053
114
HNM002 Hinman Syndrome 29 0.053
115
c BNG076 Benign Exophthalmos Syndrome 21 0.053
116
DDN005 Duodenal Somatostatinoma 20 0.053
117
AND005 Androgen Insensitivity Syndrome, Mild 19 0.053
118
AQG001 Aquagenic Pruritus 16 0.053
119
ATY026 Atypical Meigs Syndrome 10 0.053