Search results for "erythrocytosis"

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

120 hits were found for 'erythrocytosis'

# Family MCID Name MIFTS Score
1
ERY045 Erythrocytosis, Somatic 35 6.420
2
PSD044 Pseudopolycythaemia 28 5.723
3
c PRM012 Primary Polycythemia 43 5.139
4
P ERY048 Erythrocytosis, Familial, 2 17 4.540
5
c ERY032 Erythrocytosis, Familial, 4 13 4.519
6
c ERY031 Erythrocytosis, Familial, 3 12 4.519
7
ERY044 Erythrocytosis Due to Bisphosphoglycerate Mutase Deficiency 13 3.536
8
TMP008 Tempi Syndrome 12 2.930
9
CHV001 Chuvash Erythrocytosis 9 2.877
10
ATS075 Autosomal Recessive Secondary Polycythemia Not Associated with Vhl Gene 6 2.844
11
c ATS209 Autosomal Dominant Secondary Polycythemia 15 2.011
12
STR007 Stress Polycythemia 13 2.011
13
MLT106 Multiple Paragangliomas Associated with Polycythemia 9 2.011
14
ERY007 Erythropoietin Polycythemia 8 2.011
15
P PLY018 Polycythemia 58 0.217
16
PLY001 Polycythemia Vera 75 0.175
17
HMN009 Hemangioblastoma 47 0.139
18
MYM001 Myoma 46 0.129
19
HPT023 Hepatocellular Carcinoma 95 0.118
20
P HPT021 Hepatitis 55 0.118
21
THR004 Thrombocytosis 50 0.118
22
P THL005 Thalassemia 64 0.105
23
ADN018 Adenoma 55 0.105
24
RNL007 Renal Tubular Acidosis 48 0.105
25
P PRG013 Paraganglioma 46 0.105
26
NPH003 Nephrocalcinosis 41 0.105
27
CRB009 Cerebritis 33 0.105
28
VNH007 Von Hippel-Lindau Syndrome 65 0.091
29
ACN002 Acanthosis Nigricans 55 0.091
30
HYP266 Hypoxia 49 0.091
31
THR013 Thoracic Outlet Syndrome 45 0.091
32
HYP043 Hyperandrogenism 40 0.091
33
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.091
34
P ATX010 Ataxia Neuropathy Spectrum 29 0.091
35
P PHC003 Pheochromocytoma 79 0.074
36
P HMC003 Hemochromatosis 75 0.074
37
P MYL005 Myelofibrosis 68 0.074
38
P ESS003 Essential Thrombocythemia 66 0.074
39
P LKM002 Leukemia 66 0.074
40
LMY002 Leiomyoma 59 0.074
41
HYP056 Hypoglycemia 53 0.074
42
HDC001 Headache 50 0.074
43
P HYP014 Hyperuricemia 47 0.074
44
SCH016 Schimke Immunoosseous Dysplasia 46 0.074
45
SPL018 Splenomegaly 40 0.074
46
GLM011 Glomerulosclerosis 40 0.074
47
P TRC086 Trichohepatoenteric Syndrome 1 39 0.074
48
HRS011 Horseshoe Kidney 38 0.074
49
TTR016 Tetra-Amelia Syndrome 36 0.074
50
CRB085 Cerebral Hemorrhage 35 0.074
51
P MYC007 Myocardial Infarction 81 0.053
52
P APL001 Aplastic Anemia 76 0.053
53
c MLT019 Multiple Myeloma 75 0.053
54
P RNL014 Renal Cell Carcinoma 83 0.053
55
GST019 Gastrointestinal Stromal Tumor 74 0.053
56
c AMY091 Amyotrophic Lateral Sclerosis 1 82 0.053
57
CDS001 Cadasil 73 0.053
58
AND015 Androgen Insensitivity 69 0.053
59
P NRB001 Neuroblastoma 68 0.053
60
LVR012 Liver Cirrhosis 66 0.053
61
P PNM007 Pneumonia 64 0.053
62
P AMY004 Amyloidosis 63 0.053
63
P CNG401 Congenital Heart Disease 62 0.053
64
c HYP595 Hypertension, Essential 66 0.053
65
STR067 Stroke, Ischemic 65 0.053
66
P HMN010 Hemangioma 60 0.053
67
CRB039 Cerebrovascular Disease 59 0.053
68
P RCK004 Rickets 58 0.053
69
P HYP020 Hyperprolactinemia 58 0.053
70
c HPT001 Hepatitis C 57 0.053
71
P KDN018 Kidney Disease 57 0.053
72
INS024 Insulin-Like Growth Factor I 58 0.053
73
PLM033 Pulmonary Embolism 56 0.053
74
P HML002 Hemolytic Anemia 56 0.053
75
END030 End Stage Renal Failure 56 0.053
76
c ALM001 Al Amyloidosis 56 0.053
77
P INT001 Intrahepatic Cholestasis 55 0.053
78
P HYP076 Hyperthyroidism 54 0.053
79
DFC004 Deficiency Anemia 54 0.053
80
ACT105 Acute Mountain Sickness 54 0.053
81
P MYL007 Myeloma 53 0.053
82
SMT003 Somatostatinoma 53 0.053
83
P PLY014 Polycystic Kidney Disease 53 0.053
84
HPT022 Hepatoblastoma 53 0.053
85
CHL067 Cholecystitis 53 0.053
86
PTT006 Pituitary Adenoma 52 0.053
87
MYC002 Mycobacterium Avium Complex Disease 51 0.053
88
P MTH007 Methemoglobinemia 51 0.053
89
PLC003 Placental Site Trophoblastic Tumor 51 0.053
90
CHL068 Cholestasis 50 0.053
91
THY022 Thymic Carcinoma 50 0.053
92
P AXN010 Axenfeld-Rieger Syndrome, Type 3 50 0.053
93
P ADN016 Adenocarcinoma 49 0.053
94
P HYP613 Hypophosphatemic Rickets 49 0.053
95
c ACT073 Acute Leukemia 48 0.053
96
DDN006 Duodenitis 48 0.053
97
P PSD015 Pseudohypoparathyroidism 47 0.053
98
P HYD002 Hydronephrosis 45 0.053
99
P FNC004 Fanconi Syndrome 44 0.053
100
CYS016 Cystic Kidney 44 0.053
101
P LYD001 Leydig Cell Tumor 42 0.053
102
ASP007 Aspiration Pneumonia 41 0.053
103
CHL004 Cholelithiasis 40 0.053
104
VRC005 Varicose Veins 40 0.053
105
P BRS044 Breast Adenocarcinoma 39 0.053
106
NRN002 Neuronitis 36 0.053
107
HPT002 Hepatic Vein Thrombosis 35 0.053
108
MTN001 Metanephric Adenoma 35 0.053
109
P RNL017 Renal Oncocytoma 43 0.053
110
UTR039 Uterine Fibroid 34 0.053
111
FNT004 Fainting 33 0.053
112
ADS002 Adie Syndrome 30 0.053
113
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 29 0.053
114
SPR094 Sporadic Pheochromocytoma 27 0.053
115
HNM002 Hinman Syndrome 26 0.053
116
c BNG076 Benign Exophthalmos Syndrome 19 0.053
117
DDN005 Duodenal Somatostatinoma 17 0.053
118
AND005 Androgen Insensitivity Syndrome, Mild 17 0.053
119
AQG001 Aquagenic Pruritus 14 0.053
120
ATY026 Atypical Meigs Syndrome 9 0.053