Search results for "erythrocytosis"

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

147 hits were found for 'erythrocytosis'

# Family MCID Name MIFTS Score
1
ERY045 Erythrocytosis, Somatic 32 7.089
2
c PRM012 Primary Polycythemia 48 6.261
3
P ERY048 Erythrocytosis, Familial, 2 25 5.036
4
c ERY032 Erythrocytosis, Familial, 4 18 4.594
5
c ERY031 Erythrocytosis, Familial, 3 18 4.594
6
ERY044 Erythrocytosis Due to Bisphosphoglycerate Mutase Deficiency 18 3.571
7
TMP008 Tempi Syndrome 14 2.939
8
PSD044 Pseudopolycythaemia 10 2.858
9
ATS075 Autosomal Recessive Secondary Polycythemia Not Associated with Vhl Gene 6 2.858
10
CHV001 Chuvash Erythrocytosis 10 2.120
11
ERY007 Erythropoietin Polycythemia 8 2.062
12
STR007 Stress Polycythemia 15 2.021
13
c ATS209 Autosomal Dominant Secondary Polycythemia 14 2.021
14
MLT106 Multiple Paragangliomas Associated with Polycythemia 9 2.021
15
P PLY018 Polycythemia 53 0.206
16
HMN009 Hemangioblastoma 43 0.132
17
MYM001 Myoma 49 0.122
18
c CHR546 Chronic Mountain Sickness 32 0.122
19
P HRM001 Hermansky-Pudlak Syndrome 62 0.111
20
c PNC108 Pancreatitis, Hereditary 59 0.111
21
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.111
22
P HPT021 Hepatitis 58 0.111
23
HNT002 Hantavirus Pulmonary Syndrome 52 0.111
24
THR004 Thrombocytosis 48 0.111
25
ANR002 Aniridia 72 0.100
26
P THL005 Thalassemia 56 0.100
27
ADN018 Adenoma 54 0.100
28
ACN002 Acanthosis Nigricans 53 0.100
29
RNL007 Renal Tubular Acidosis 46 0.100
30
P PRG013 Paraganglioma 41 0.100
31
NPH003 Nephrocalcinosis 39 0.100
32
CRB009 Cerebritis 37 0.100
33
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.100
34
P ATX010 Ataxia Neuropathy Spectrum 31 0.100
35
HPT023 Hepatocellular Carcinoma 90 0.086
36
VNH007 Von Hippel-Lindau Syndrome 68 0.086
37
THR013 Thoracic Outlet Syndrome 47 0.086
38
HYP266 Hypoxia 42 0.086
39
HYP043 Hyperandrogenism 40 0.086
40
P PHC003 Pheochromocytoma 76 0.071
41
P HMC003 Hemochromatosis 75 0.071
42
P CNG401 Congenital Heart Disease 68 0.071
43
STR067 Stroke, Ischemic 68 0.071
44
P MYL005 Myelofibrosis 64 0.071
45
P ESS003 Essential Thrombocythemia 63 0.071
46
P LKM002 Leukemia 61 0.071
47
P RSP003 Respiratory Failure 58 0.071
48
SCH016 Schimke Immunoosseous Dysplasia 51 0.071
49
HYP056 Hypoglycemia 49 0.071
50
LMY002 Leiomyoma 49 0.071
51
P ACT105 Acute Mountain Sickness 46 0.071
52
P HYP014 Hyperuricemia 45 0.071
53
HDC001 Headache 42 0.071
54
P TRC086 Trichohepatoenteric Syndrome 1 42 0.071
55
TTR016 Tetra-Amelia Syndrome 38 0.071
56
GLM011 Glomerulosclerosis 38 0.071
57
ADS002 Adie Syndrome 34 0.071
58
SPL018 Splenomegaly 34 0.071
59
CRB085 Cerebral Hemorrhage 31 0.071
60
HPT074 Hepatic Adenoma, Somatic 30 0.071
61
HRS011 Horseshoe Kidney 29 0.071
62
HNM002 Hinman Syndrome 27 0.071
63
c AMY091 Amyotrophic Lateral Sclerosis 1 83 0.050
64
P RNL014 Renal Cell Carcinoma 81 0.050
65
c MLT019 Multiple Myeloma 77 0.050
66
P MYC007 Myocardial Infarction 76 0.050
67
P NRB001 Neuroblastoma 73 0.050
68
CDS001 Cadasil 70 0.050
69
P APL001 Aplastic Anemia 70 0.050
70
c HYP595 Hypertension, Essential 68 0.050
71
GST019 Gastrointestinal Stromal Tumor 68 0.050
72
AND015 Androgen Insensitivity 65 0.050
73
CNG034 Congestive Heart Failure 65 0.050
74
c HPT001 Hepatitis C 64 0.050
75
INS024 Insulin-Like Growth Factor I 64 0.050
76
PLY125 Polycythemia Vera, Somatic 62 0.050
77
P AMY004 Amyloidosis 60 0.050
78
P AXN010 Axenfeld-Rieger Syndrome, Type 3 60 0.050
79
P PLY014 Polycystic Kidney Disease 60 0.050
80
LVR012 Liver Cirrhosis 59 0.050
81
CRB039 Cerebrovascular Disease 58 0.050
82
P KDN018 Kidney Disease 57 0.050
83
P ADN016 Adenocarcinoma 56 0.050
84
P PNM007 Pneumonia 56 0.050
85
P HYP020 Hyperprolactinemia 56 0.050
86
P RCK004 Rickets 55 0.050
87
P HMN010 Hemangioma 54 0.050
88
P MYL007 Myeloma 54 0.050
89
PLM033 Pulmonary Embolism 53 0.050
90
P HML002 Hemolytic Anemia 52 0.050
91
DFC004 Deficiency Anemia 52 0.050
92
END030 End Stage Renal Failure 51 0.050
93
CHL067 Cholecystitis 51 0.050
94
c ACT073 Acute Leukemia 49 0.050
95
P HYP613 Hypophosphatemic Rickets 49 0.050
96
P INT001 Intrahepatic Cholestasis 49 0.050
97
HPT022 Hepatoblastoma 49 0.050
98
MGR028 Migraine with or Without Aura 1 49 0.050
99
P RNL017 Renal Oncocytoma 48 0.050
100
P HYP076 Hyperthyroidism 48 0.050
101
THY022 Thymic Carcinoma 48 0.050
102
THR016 Thrombophlebitis 48 0.050
103
ISC004 Ischemia 47 0.050
104
P FNC004 Fanconi Syndrome 46 0.050
105
MYC002 Mycobacterium Avium Complex Disease 46 0.050
106
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.050
107
c ALM001 Al Amyloidosis 45 0.050
108
PLC003 Placental Site Trophoblastic Tumor 45 0.050
109
UTR039 Uterine Fibroid 45 0.050
110
CHL068 Cholestasis 45 0.050
111
PTT006 Pituitary Adenoma 45 0.050
112
SMT003 Somatostatinoma 44 0.050
113
P MTH007 Methemoglobinemia 44 0.050
114
CYS016 Cystic Kidney 43 0.050
115
P MGS004 Meige Syndrome 43 0.050
116
P BRS044 Breast Adenocarcinoma 43 0.050
117
c PND001 Pain Disorder 43 0.050
118
P PSD015 Pseudohypoparathyroidism 42 0.050
119
P HYD002 Hydronephrosis 42 0.050
120
ACT098 Acute Erythroid Leukemia 41 0.050
121
NRN002 Neuronitis 40 0.050
122
CHL004 Cholelithiasis 40 0.050
123
DDN006 Duodenitis 40 0.050
124
P LYD001 Leydig Cell Tumor 38 0.050
125
CHR010 Chorioangioma 37 0.050
126
ASP007 Aspiration Pneumonia 37 0.050
127
RSP006 Respiratory System Disease 36 0.050
128
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 33 0.050
129
c GLL024 Gallbladder Disease 1 33 0.050
130
MLT001 Multiple Chemical Sensitivity 33 0.050
131
HPT002 Hepatic Vein Thrombosis 32 0.050
132
c SPR094 Sporadic Pheochromocytoma 31 0.050
133
c ACQ010 Acquired Polycythemia 31 0.050
134
DDN005 Duodenal Somatostatinoma 29 0.050
135
MTN001 Metanephric Adenoma 28 0.050
136
FNT004 Fainting 27 0.050
137
BLD054 Blood Protein Disease 24 0.050
138
ALR002 Al-Raqad Syndrome 23 0.050
139
c BNG076 Benign Exophthalmos Syndrome 21 0.050
140
AND005 Androgen Insensitivity Syndrome, Mild 19 0.050
141
PHY001 Physiological Polycythemia 17 0.050
142
CNT017 Central Nervous System Origin Vertigo 17 0.050
143
AQG001 Aquagenic Pruritus 14 0.050
144
c ATS229 Autosomal Recessive Lymphoproliferative Disease 11 0.050
145
ATY026 Atypical Meigs Syndrome 10 0.050
146
c CRN178 Coronary Heart Disease 6 10 0.050
147
c CRN173 Coronary Heart Disease 8 9 0.050