Search results for "hematopoiesis"

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

163 hits were found for 'hematopoiesis'

# Family MCID Name MIFTS Score
1
NTR040 Neutropenia, Cyclic 49 5.814
2
P LKM002 Leukemia 61 0.321
3
P APL001 Aplastic Anemia 70 0.213
4
P MYL005 Myelofibrosis 64 0.213
5
P THL005 Thalassemia 56 0.193
6
MYL009 Myelodysplastic Syndrome 69 0.170
7
P MYL006 Myeloid Leukemia 59 0.164
8
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 48 0.164
9
HMG002 Hemoglobinuria 39 0.164
10
P HRD011 Hereditary Spherocytosis 52 0.151
11
P PLY018 Polycythemia 53 0.111
12
END072 Endotheliitis 39 0.111
13
P OST001 Osteopetrosis 63 0.102
14
P BRS047 Breast Cancer 100 0.091
15
HMT018 Hematopoietic Stem Cell Transplantation 45 0.091
16
c HMG003 Hemoglobin E Disease 35 0.091
17
SPL018 Splenomegaly 34 0.091
18
MDS022 Mediastinitis 33 0.091
19
P NTR004 Neutropenia 50 0.079
20
c ACT073 Acute Leukemia 49 0.079
21
P PNC001 Pancytopenia 41 0.079
22
P CNG003 Congenital Dyserythropoietic Anemia 37 0.079
23
PYG006 Pyogenic Granuloma 37 0.079
24
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 22 0.079
25
HV1006 Hiv-1 77 0.064
26
c MLT019 Multiple Myeloma 77 0.064
27
SVR004 Severe Combined Immunodeficiency 65 0.064
28
PYR013 Pyruvate Kinase Deficiency 59 0.064
29
P MYL007 Myeloma 54 0.064
30
HPT022 Hepatoblastoma 49 0.064
31
THR004 Thrombocytosis 48 0.064
32
CYT008 Cytomegalovirus Infection 47 0.064
33
CHR285 Chronic Myelomonocytic Leukemia 44 0.064
34
PRN011 Pernicious Anemia 44 0.064
35
HMN009 Hemangioblastoma 43 0.064
36
PRP016 Paraplegia 41 0.064
37
P TCL004 T-Cell Leukemia 40 0.064
38
MCR017 Macrocytic Anemia 39 0.064
39
RFR010 Refractory Anemia 38 0.064
40
P SDR003 Sideroblastic Anemia 38 0.064
41
P HMG021 Hemoglobin E - Beta-Thalassemia 28 0.064
42
c NTR033 Neutropenia, Severe Congenital 1, Autosomal Dominant 27 0.064
43
MN1001 Mn1 25 0.064
44
P PRS040 Prostate Cancer 90 0.045
45
P OBS005 Obesity 89 0.045
46
P RHM011 Rheumatoid Arthritis 88 0.045
47
P PLM037 Pulmonary Hypertension 78 0.045
48
P DMN001 Diamond-Blackfan Anemia 66 0.045
49
TBR010 Tuberculosis 64 0.045
50
P GCH001 Gaucher's Disease 64 0.045
51
P ESS003 Essential Thrombocythemia 63 0.045
52
LNG024 Langerhans-Cell Histiocytosis 63 0.045
53
P HLP001 Holoprosencephaly 62 0.045
54
DWN001 Down Syndrome 62 0.045
55
P FLL037 Follicular Lymphoma 62 0.045
56
PLY125 Polycythemia Vera, Somatic 62 0.045
57
CHD001 Chediak-Higashi Syndrome 61 0.045
58
P ART022 Arthritis 61 0.045
59
PRT036 Peritonitis 58 0.045
60
P HPT021 Hepatitis 58 0.045
61
P LYM026 Lymphoblastic Leukemia 57 0.045
62
P RTH001 Rothmund-Thomson Syndrome 57 0.045
63
P KDN018 Kidney Disease 57 0.045
64
SRC014 Sarcoma 57 0.045
65
P ASP006 Aspergillosis 56 0.045
66
P ADN016 Adenocarcinoma 56 0.045
67
P AST007 Astrocytoma 55 0.045
68
ADN018 Adenoma 54 0.045
69
HMT002 Hematologic Cancer 53 0.045
70
GRY002 Gray Platelet Syndrome 53 0.045
71
APP008 Appendicitis 52 0.045
72
c PRC016 Pre-Eclampsia 51 0.045
73
LST001 Listeriosis 51 0.045
74
P ESP024 Esophagitis 51 0.045
75
P PNC044 Pancreatitis 51 0.045
76
P MNN013 Meningitis 51 0.045
77
P HST010 Histiocytosis 51 0.045
78
P FBR017 Fibrosarcoma 50 0.045
79
ATH003 Atherosclerosis 50 0.045
80
BNC003 Bone Cancer 50 0.045
81
P THR014 Thrombocytopenia 50 0.045
82
HYD012 Hydrops Fetalis 50 0.045
83
TNG003 Tongue Cancer 50 0.045
84
P HYP098 Hypereosinophilic Syndrome 49 0.045
85
P THY032 Thyroiditis 48 0.045
86
P ESN007 Eosinophilia 48 0.045
87
c ADL017 Adult T-Cell Leukemia 48 0.045
88
THY022 Thymic Carcinoma 48 0.045
89
HMR001 Hemorrhagic Thrombocythemia 48 0.045
90
P TMT001 Timothy Syndrome 48 0.045
91
P CTR002 Cataract 48 0.045
92
BNM001 Bone Marrow Cancer 47 0.045
93
DPH001 Diphtheria 47 0.045
94
P ECL001 Eclampsia 47 0.045
95
PLS011 Plasmacytoma 46 0.045
96
P ENC008 Encephalocele 46 0.045
97
LYM022 Lymphangioma 46 0.045
98
EXF001 Exfoliation Syndrome 45 0.045
99
P MNC007 Monocytic Leukemia 45 0.045
100
P INT070 Intestinal Obstruction 45 0.045
101
P CNT005 Central Nervous System Lymphoma 44 0.045
102
CSY001 C Syndrome 44 0.045
103
GRN039 Greenberg Skeletal Dysplasia 43 0.045
104
ADL002 Adult Syndrome 43 0.045
105
P ATX004 Ataxia 43 0.045
106
PRR002 Pure Red-Cell Aplasia 43 0.045
107
P PLC011 Pilocytic Astrocytoma 42 0.045
108
NDL013 Nodular Regenerative Hyperplasia 42 0.045
109
c HMN021 Human T-Cell Leukemia Virus Type 1 42 0.045
110
DWR001 Dwarfism 42 0.045
111
EPT020 Epithelioid Hemangioendothelioma 42 0.045
112
PNM008 Pneumothorax 41 0.045
113
P EXN002 Exanthem 41 0.045
114
HMS001 Hemosiderosis 40 0.045
115
c INV001 Invasive Aspergillosis 40 0.045
116
CHR005 Chorioamnionitis 40 0.045
117
EXT010 Extramedullary Plasmacytoma 40 0.045
118
c CHR092 Chronic Myeloproliferative Disease 39 0.045
119
BNF002 Bone Fracture 39 0.045
120
MYL001 Myelitis 39 0.045
121
NTR003 Natural Killer Cell Leukemia 38 0.045
122
FLL031 Follicular Adenoma 37 0.045
123
CHR008 Choroiditis 37 0.045
124
c MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 37 0.045
125
CNG105 Congenital Lobar Emphysema 36 0.045
126
MSS002 Mass Syndrome 36 0.045
127
P PLN008 Peeling Skin Syndrome 36 0.045
128
VSC047 Vascular Malformation 35 0.045
129
HST016 Histiocytic Sarcoma 35 0.045
130
HMN016 Hemangioendothelioma 35 0.045
131
XLN003 X-Linked Sideroblastic Anemia with Ataxia 34 0.045
132
OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 33 0.045
133
c OST126 Osteopetrosis, Autosomal Recessive 1 33 0.045
134
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 33 0.045
135
FBR002 Fibrosarcoma of Bone 33 0.045
136
BLD053 Blood Platelet Disease 32 0.045
137
c NTR038 Neutropenia, Severe Congenital 3, Autosomal Recessive 31 0.045
138
c NTR039 Neutropenia, Severe Congenital 4, Autosomal Recessive 30 0.045
139
LYM095 Lymphangiomatosis 29 0.045
140
c PRM023 Pre-Malignant Neoplasm 29 0.045
141
SVR077 Severe Combined Immune Deficiency 29 0.045
142
CNG069 Congenital Cytomegalovirus 28 0.045
143
P GGN002 Gigantism 28 0.045
144
LKC003 Leukocyte Disease 28 0.045
145
c OST129 Osteopetrosis, Autosomal Recessive 2 28 0.045
146
P MSN006 Mesenchymoma 28 0.045
147
NTR036 Neutropenia, Severe Congenital, X-Linked 26 0.045
148
PRS024 Parasagittal Meningioma 26 0.045
149
c PLN018 Peeling Skin Syndrome 2 25 0.045
150
c BNG012 Benign Mesenchymoma 25 0.045
151
HMX002 Heme Oxygenase-1 Deficiency 25 0.045
152
DFF022 Diffuse Neonatal Hemangiomatosis 24 0.045
153
c PLN017 Peeling Skin Syndrome 1 23 0.045
154
TNG004 Tongue Disease 23 0.045
155
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 21 0.045
156
BNM011 Bone Marrow Failure Syndrome 2 20 0.045
157
c NTR034 Neutropenia, Severe Congenital, 6, Autosomal Recessive 19 0.045
158
c NTR037 Neutropenia, Severe Congenital 2, Autosomal Dominant 19 0.045
159
c PRX067 Paroxysmal Nocturnal Hemoglobinuria 2 16 0.045
160
RDT014 Radiation Myelitis 16 0.045
161
CHK002 Cheek Mucosa Cancer 9 0.045
162
WHT007 White Platelet Syndrome 8 0.045
163
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 5 0.045