Search results for "hematopoiesis"

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

182 hits were found for 'hematopoiesis'

# Family MCID Name MIFTS Score
1
NTR040 Neutropenia, Cyclic 50 5.786
2
P LKM002 Leukemia 70 0.310
3
P MYL005 Myelofibrosis 67 0.212
4
P APL001 Aplastic Anemia 73 0.208
5
P THL005 Thalassemia 61 0.194
6
MYL009 Myelodysplastic Syndrome 74 0.173
7
P MYL006 Myeloid Leukemia 67 0.162
8
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.162
9
HMG002 Hemoglobinuria 49 0.162
10
P HRD011 Hereditary Spherocytosis 53 0.144
11
P PLY018 Polycythemia 57 0.106
12
END072 Endotheliitis 42 0.106
13
HMT018 Hematopoietic Stem Cell Transplantation 41 0.106
14
P OST001 Osteopetrosis 62 0.097
15
P BRS047 Breast Cancer 100 0.087
16
P LYM118 Lymphoma 70 0.087
17
c ACT073 Acute Leukemia 62 0.087
18
SPL018 Splenomegaly 44 0.087
19
MDS022 Mediastinitis 41 0.087
20
THL017 Thalassemia Intermedia 40 0.087
21
P NTR004 Neutropenia 59 0.075
22
BNM001 Bone Marrow Cancer 52 0.075
23
P PNC001 Pancytopenia 52 0.075
24
P TCL004 T-Cell Leukemia 46 0.075
25
c HMG003 Hemoglobin E Disease 44 0.075
26
c PRM023 Pre-Malignant Neoplasm 43 0.075
27
PYG006 Pyogenic Granuloma 41 0.075
28
P CNG003 Congenital Dyserythropoietic Anemia 39 0.075
29
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 29 0.075
30
MRG013 Mirage Syndrome 26 0.075
31
HV1006 Hiv-1 82 0.061
32
P MLT019 Multiple Myeloma 80 0.061
33
SVR004 Severe Combined Immunodeficiency 68 0.061
34
P ESS003 Essential Thrombocythemia 68 0.061
35
HMT002 Hematologic Cancer 64 0.061
36
PYR013 Pyruvate Kinase Deficiency 58 0.061
37
c ADL017 Adult T-Cell Leukemia 58 0.061
38
CHR285 Chronic Myelomonocytic Leukemia 55 0.061
39
THR004 Thrombocytosis 55 0.061
40
HPT022 Hepatoblastoma 53 0.061
41
CYT008 Cytomegalovirus Infection 51 0.061
42
CSY001 C Syndrome 49 0.061
43
PRP016 Paraplegia 49 0.061
44
BNF002 Bone Fracture 47 0.061
45
PRN011 Pernicious Anemia 46 0.061
46
RFR010 Refractory Anemia 45 0.061
47
BNC003 Bone Cancer 45 0.061
48
HMN009 Hemangioblastoma 45 0.061
49
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.061
50
THL018 Thalassemia Major 42 0.061
51
MCR017 Macrocytic Anemia 41 0.061
52
P SDR003 Sideroblastic Anemia 39 0.061
53
MN1001 Mn1 31 0.061
54
c NTR033 Neutropenia, Severe Congenital 1, Autosomal Dominant 21 0.061
55
P OBS005 Obesity 93 0.043
56
P PRS040 Prostate Cancer 89 0.043
57
P RHM011 Rheumatoid Arthritis 88 0.043
58
P PLM037 Pulmonary Hypertension 79 0.043
59
P ART022 Arthritis 75 0.043
60
c LKM061 Leukemia, Acute Myeloid 71 0.043
61
P HPT021 Hepatitis 70 0.043
62
P ADN016 Adenocarcinoma 69 0.043
63
TBR010 Tuberculosis 69 0.043
64
P DMN001 Diamond-Blackfan Anemia 68 0.043
65
PCK002 Pick Disease 67 0.043
66
SRC014 Sarcoma 66 0.043
67
P FLL037 Follicular Lymphoma 66 0.043
68
P AST007 Astrocytoma 65 0.043
69
P MNN013 Meningitis 65 0.043
70
DWN001 Down Syndrome 65 0.043
71
P OST002 Osteoporosis 64 0.043
72
P THR014 Thrombocytopenia 64 0.043
73
CHD001 Chediak-Higashi Syndrome 64 0.043
74
P DYS007 Dyskeratosis Congenita 63 0.043
75
PLY125 Polycythemia Vera, Somatic 63 0.043
76
P HLP001 Holoprosencephaly 62 0.043
77
ATH003 Atherosclerosis 62 0.043
78
PRT036 Peritonitis 62 0.043
79
P ESP024 Esophagitis 62 0.043
80
OCL009 Ocular Cancer 62 0.043
81
P ESN007 Eosinophilia 61 0.043
82
WLL001 Williams-Beuren Syndrome 61 0.043
83
P ASP006 Aspergillosis 60 0.043
84
P HMN010 Hemangioma 60 0.043
85
P PNC044 Pancreatitis 60 0.043
86
P LYM026 Lymphoblastic Leukemia 60 0.043
87
APP008 Appendicitis 60 0.043
88
TNG003 Tongue Cancer 60 0.043
89
MSS002 Mass Syndrome 59 0.043
90
ADN018 Adenoma 59 0.043
91
P PLC011 Pilocytic Astrocytoma 58 0.043
92
DPH001 Diphtheria 58 0.043
93
P CTR002 Cataract 57 0.043
94
P RTH001 Rothmund-Thomson Syndrome 57 0.043
95
EXF001 Exfoliation Syndrome 57 0.043
96
P EXN002 Exanthem 57 0.043
97
P INT070 Intestinal Obstruction 56 0.043
98
P TMT001 Timothy Syndrome 56 0.043
99
P FBR017 Fibrosarcoma 56 0.043
100
PLS011 Plasmacytoma 56 0.043
101
GRY002 Gray Platelet Syndrome 55 0.043
102
P HST010 Histiocytosis 55 0.043
103
P MNC007 Monocytic Leukemia 55 0.043
104
LST001 Listeriosis 54 0.043
105
P ECL001 Eclampsia 54 0.043
106
P THY032 Thyroiditis 54 0.043
107
LYM022 Lymphangioma 54 0.043
108
P HYP345 Hyper-Ige Recurrent Infection Syndrome 54 0.043
109
ADL002 Adult Syndrome 53 0.043
110
P ATX004 Ataxia 53 0.043
111
P CNT005 Central Nervous System Lymphoma 53 0.043
112
PNM008 Pneumothorax 52 0.043
113
c HMN021 Human T-Cell Leukemia Virus Type 1 51 0.043
114
P HYP098 Hypereosinophilic Syndrome 51 0.043
115
NDL013 Nodular Regenerative Hyperplasia 49 0.043
116
EXT010 Extramedullary Plasmacytoma 49 0.043
117
MYL001 Myelitis 48 0.043
118
CHR005 Chorioamnionitis 48 0.043
119
c INV001 Invasive Aspergillosis 47 0.043
120
P ENC008 Encephalocele 47 0.043
121
LKC003 Leukocyte Disease 47 0.043
122
NTR003 Natural Killer Cell Leukemia 47 0.043
123
P PLN008 Peeling Skin Syndrome 47 0.043
124
DWR001 Dwarfism 46 0.043
125
PRR002 Pure Red-Cell Aplasia 46 0.043
126
BLD053 Blood Platelet Disease 46 0.043
127
NPH003 Nephrocalcinosis 46 0.043
128
VSC047 Vascular Malformation 45 0.043
129
EPT020 Epithelioid Hemangioendothelioma 45 0.043
130
HMS001 Hemosiderosis 45 0.043
131
HYD012 Hydrops Fetalis 44 0.043
132
CRD001 Cardiac Tamponade 44 0.043
133
CHR008 Choroiditis 43 0.043
134
c CHR064 Chronic Monocytic Leukemia 43 0.043
135
IMM127 Immune System Cancer 42 0.043
136
BND014 Bone Development Disease 42 0.043
137
FBR002 Fibrosarcoma of Bone 41 0.043
138
FLL031 Follicular Adenoma 41 0.043
139
c NTR038 Neutropenia, Severe Congenital 3, Autosomal Recessive 41 0.043
140
TNG004 Tongue Disease 41 0.043
141
HST016 Histiocytic Sarcoma 40 0.043
142
SPC003 Specific Developmental Disorder 40 0.043
143
ACT113 Acute Myeloblastic Leukemia with Maturation 40 0.043
144
c ACT020 Acute T Cell Leukemia 39 0.043
145
GRN039 Greenberg Skeletal Dysplasia 38 0.043
146
THL010 Thalassemia Minor 38 0.043
147
HMN016 Hemangioendothelioma 38 0.043
148
BNS002 Bone Structure Disease 36 0.043
149
SVR077 Severe Combined Immune Deficiency 36 0.043
150
BNT003 Bent Bone Dysplasia Syndrome 36 0.043
151
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 36 0.043
152
ACR002 Acrocapitofemoral Dysplasia 36 0.043
153
c PLN018 Peeling Skin Syndrome 2 35 0.043
154
CNG069 Congenital Cytomegalovirus 34 0.043
155
P MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 34 0.043
156
c PLN017 Peeling Skin Syndrome 1 33 0.043
157
LYM095 Lymphangiomatosis 33 0.043
158
c OST126 Osteopetrosis, Autosomal Recessive 1 33 0.043
159
c OST129 Osteopetrosis, Autosomal Recessive 2 33 0.043
160
P MSN006 Mesenchymoma 32 0.043
161
OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 30 0.043
162
ACT114 Acute Myeloblastic Leukemia Without Maturation 30 0.043
163
HNS001 Hansen's Disease 29 0.043
164
ACT118 Acute Non Lymphoblastic Leukemia 29 0.043
165
NTR036 Neutropenia, Severe Congenital, X-Linked 28 0.043
166
c NTR039 Neutropenia, Severe Congenital 4, Autosomal Recessive 28 0.043
167
OST097 Osteoporotic Fracture 27 0.043
168
GGN002 Gigantism 27 0.043
169
c BNG012 Benign Mesenchymoma 26 0.043
170
BNM011 Bone Marrow Failure Syndrome 2 26 0.043
171
PRS024 Parasagittal Meningioma 25 0.043
172
HMX002 Heme Oxygenase-1 Deficiency 25 0.043
173
c PRX067 Paroxysmal Nocturnal Hemoglobinuria 2 23 0.043
174
DFF022 Diffuse Neonatal Hemangiomatosis 21 0.043
175
c NTR034 Neutropenia, Severe Congenital, 6, Autosomal Recessive 21 0.043
176
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 20 0.043
177
c NTR037 Neutropenia, Severe Congenital 2, Autosomal Dominant 20 0.043
178
WHT007 White Platelet Syndrome 18 0.043
179
RDT014 Radiation Myelitis 18 0.043
180
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 17 0.043
181
CHK002 Cheek Mucosa Cancer 15 0.043
182
c NTR043 Neutropenia, Severe Congenital 7, Autosomal Recessive 11 0.043