Search results for "hematopoiesis"

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

190 hits were found for 'hematopoiesis'

# Family MCID Name MIFTS Score
1
NTR040 Neutropenia, Cyclic 51 5.785
2
P LKM002 Leukemia 70 0.305
3
P APL001 Aplastic Anemia 74 0.205
4
P MYL005 Myelofibrosis 67 0.205
5
P THL005 Thalassemia 61 0.186
6
MYL009 Myelodysplastic Syndrome 73 0.171
7
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 59 0.160
8
P MYL006 Myeloid Leukemia 67 0.160
9
HMG002 Hemoglobinuria 49 0.160
10
P HRD011 Hereditary Spherocytosis 51 0.142
11
P PLY018 Polycythemia 58 0.105
12
END072 Endotheliitis 41 0.105
13
P OST001 Osteopetrosis 63 0.096
14
HMT018 Hematopoietic Stem Cell Transplantation 39 0.096
15
P BRS047 Breast Cancer 100 0.085
16
P LYM118 Lymphoma 68 0.085
17
c ACT073 Acute Leukemia 61 0.085
18
SPL018 Splenomegaly 45 0.085
19
MDS022 Mediastinitis 37 0.085
20
BNM001 Bone Marrow Cancer 56 0.074
21
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 28 0.074
22
SPN041 Spinal Cord Disease 50 0.074
23
P NTR004 Neutropenia 59 0.074
24
P CNG003 Congenital Dyserythropoietic Anemia 38 0.074
25
c HMG003 Hemoglobin E Disease 44 0.074
26
P PNC001 Pancytopenia 53 0.074
27
PYG006 Pyogenic Granuloma 47 0.074
28
P TCL004 T-Cell Leukemia 44 0.074
29
THL017 Thalassemia Intermedia 38 0.074
30
c PRM023 Pre-Malignant Neoplasm 42 0.074
31
c MLT019 Multiple Myeloma 77 0.060
32
HV1006 Hiv-1 80 0.060
33
P ESS003 Essential Thrombocythemia 66 0.060
34
PYR013 Pyruvate Kinase Deficiency 58 0.060
35
CSY001 C Syndrome 49 0.060
36
SVR004 Severe Combined Immunodeficiency 71 0.060
37
BNC003 Bone Cancer 44 0.060
38
HMT002 Hematologic Cancer 62 0.060
39
PRP016 Paraplegia 49 0.060
40
c CHR285 Chronic Myelomonocytic Leukemia 54 0.060
41
c ADL017 Adult T-Cell Leukemia 59 0.060
42
HPT022 Hepatoblastoma 57 0.060
43
THR004 Thrombocytosis 55 0.060
44
PRN011 Pernicious Anemia 41 0.060
45
MCR017 Macrocytic Anemia 43 0.060
46
P SDR003 Sideroblastic Anemia 40 0.060
47
c NTR033 Neutropenia, Severe Congenital 1, Autosomal Dominant 25 0.060
48
HMN009 Hemangioblastoma 45 0.060
49
P MYL007 Myeloma 52 0.060
50
CYT008 Cytomegalovirus Infection 51 0.060
51
RFR010 Refractory Anemia 43 0.060
52
THL018 Thalassemia Major 31 0.060
53
BNF002 Bone Fracture 46 0.060
54
MN1001 Mn1 28 0.060
55
P PRS040 Prostate Cancer 89 0.043
56
P OBS005 Obesity 91 0.043
57
c LKM061 Leukemia, Acute Myeloid 71 0.043
58
P RHM011 Rheumatoid Arthritis 87 0.043
59
GRN039 Greenberg Skeletal Dysplasia 40 0.043
60
P OST002 Osteoporosis 63 0.043
61
PLY125 Polycythemia Vera, Somatic 63 0.043
62
P GCH001 Gaucher's Disease 63 0.043
63
WLL001 Williams-Beuren Syndrome 61 0.043
64
CHD001 Chediak-Higashi Syndrome 66 0.043
65
P HYP345 Hyper-Ige Recurrent Infection Syndrome 54 0.043
66
P PLM037 Pulmonary Hypertension 78 0.043
67
P KDN018 Kidney Disease 64 0.043
68
P DYS007 Dyskeratosis Congenita 64 0.043
69
PCK002 Pick Disease 66 0.043
70
P RTH001 Rothmund-Thomson Syndrome 56 0.043
71
P TMT001 Timothy Syndrome 58 0.043
72
P DMN001 Diamond-Blackfan Anemia 69 0.043
73
OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 31 0.043
74
TBR010 Tuberculosis 70 0.043
75
DWN001 Down Syndrome 65 0.043
76
LNG024 Langerhans-Cell Histiocytosis 64 0.043
77
c OST126 Osteopetrosis, Autosomal Recessive 1 34 0.043
78
P ART022 Arthritis 73 0.043
79
c MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 35 0.043
80
P HPT021 Hepatitis 74 0.043
81
c NTR038 Neutropenia, Severe Congenital 3, Autosomal Recessive 42 0.043
82
ADL002 Adult Syndrome 53 0.043
83
P ASP006 Aspergillosis 61 0.043
84
c PLN018 Peeling Skin Syndrome 2 36 0.043
85
GRY002 Gray Platelet Syndrome 55 0.043
86
c NTR039 Neutropenia, Severe Congenital 4, Autosomal Recessive 28 0.043
87
c OST129 Osteopetrosis, Autosomal Recessive 2 33 0.043
88
BNT003 Bent Bone Dysplasia Syndrome 37 0.043
89
PRT036 Peritonitis 65 0.043
90
NTR036 Neutropenia, Severe Congenital, X-Linked 28 0.043
91
P AST007 Astrocytoma 66 0.043
92
XLN003 X-Linked Sideroblastic Anemia with Ataxia 32 0.043
93
P INT070 Intestinal Obstruction 55 0.043
94
MSS002 Mass Syndrome 49 0.043
95
TNG004 Tongue Disease 40 0.043
96
P HLP001 Holoprosencephaly 62 0.043
97
HYD012 Hydrops Fetalis 45 0.043
98
LST001 Listeriosis 53 0.043
99
EXF001 Exfoliation Syndrome 56 0.043
100
SRC014 Sarcoma 66 0.043
101
APP008 Appendicitis 61 0.043
102
P HMN010 Hemangioma 62 0.043
103
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 37 0.043
104
ATH003 Atherosclerosis 63 0.043
105
P ESN007 Eosinophilia 61 0.043
106
P ENC008 Encephalocele 48 0.043
107
P ECL001 Eclampsia 55 0.043
108
P MNN013 Meningitis 66 0.043
109
ACR002 Acrocapitofemoral Dysplasia 35 0.043
110
TNG003 Tongue Cancer 59 0.043
111
c NTR034 Neutropenia, Severe Congenital, 6, Autosomal Recessive 21 0.043
112
OCL009 Ocular Cancer 61 0.043
113
P ESP024 Esophagitis 62 0.043
114
P LYM026 Lymphoblastic Leukemia 60 0.043
115
c PRC016 Pre-Eclampsia 57 0.043
116
P PLC011 Pilocytic Astrocytoma 59 0.043
117
HMR001 Hemorrhagic Thrombocythemia 47 0.043
118
NTR003 Natural Killer Cell Leukemia 46 0.043
119
P HST010 Histiocytosis 56 0.043
120
P FLL037 Follicular Lymphoma 68 0.043
121
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 20 0.043
122
P PNC044 Pancreatitis 62 0.043
123
P HYP098 Hypereosinophilic Syndrome 48 0.043
124
P ADN016 Adenocarcinoma 69 0.043
125
c NTR037 Neutropenia, Severe Congenital 2, Autosomal Dominant 20 0.043
126
c PLN017 Peeling Skin Syndrome 1 32 0.043
127
PNM008 Pneumothorax 51 0.043
128
DPH001 Diphtheria 55 0.043
129
BNM011 Bone Marrow Failure Syndrome 2 29 0.043
130
P CTR002 Cataract 57 0.043
131
DWR001 Dwarfism 42 0.043
132
LYM022 Lymphangioma 55 0.043
133
c CHR092 Chronic Myeloproliferative Disease 50 0.043
134
PRR002 Pure Red-Cell Aplasia 47 0.043
135
P FBR017 Fibrosarcoma 55 0.043
136
P THR014 Thrombocytopenia 63 0.043
137
NPH003 Nephrocalcinosis 47 0.043
138
P PLN008 Peeling Skin Syndrome 45 0.043
139
c PRX067 Paroxysmal Nocturnal Hemoglobinuria 2 22 0.043
140
P THY032 Thyroiditis 57 0.043
141
PLS011 Plasmacytoma 57 0.043
142
HMX002 Heme Oxygenase-1 Deficiency 25 0.043
143
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.043
144
c ACT020 Acute T Cell Leukemia 38 0.043
145
ACT113 Acute Myeloblastic Leukemia with Maturation 40 0.043
146
ADN018 Adenoma 59 0.043
147
NDL013 Nodular Regenerative Hyperplasia 46 0.043
148
HMS001 Hemosiderosis 42 0.043
149
SXL003 Sexual Disorder 45 0.043
150
P ATX004 Ataxia 53 0.043
151
ACT114 Acute Myeloblastic Leukemia Without Maturation 29 0.043
152
P EXN002 Exanthem 57 0.043
153
P CNT005 Central Nervous System Lymphoma 51 0.043
154
BLD053 Blood Platelet Disease 44 0.043
155
LKC003 Leukocyte Disease 45 0.043
156
CRD001 Cardiac Tamponade 43 0.043
157
CHK002 Cheek Mucosa Cancer 14 0.043
158
P MNC007 Monocytic Leukemia 52 0.043
159
ACT118 Acute Non Lymphoblastic Leukemia 27 0.043
160
EXT010 Extramedullary Plasmacytoma 49 0.043
161
c HMN021 Human T-Cell Leukemia Virus Type 1 51 0.043
162
SPC003 Specific Developmental Disorder 39 0.043
163
EPT020 Epithelioid Hemangioendothelioma 46 0.043
164
MYL001 Myelitis 35 0.043
165
FLL031 Follicular Adenoma 40 0.043
166
c CHR064 Chronic Monocytic Leukemia 42 0.043
167
CHR008 Choroiditis 43 0.043
168
HST016 Histiocytic Sarcoma 38 0.043
169
HNS001 Hansen's Disease 30 0.043
170
PRS024 Parasagittal Meningioma 26 0.043
171
WHT007 White Platelet Syndrome 17 0.043
172
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 16 0.043
173
DFF022 Diffuse Neonatal Hemangiomatosis 22 0.043
174
GGN002 Gigantism 29 0.043
175
c BNG012 Benign Mesenchymoma 25 0.043
176
CHR005 Chorioamnionitis 47 0.043
177
BND014 Bone Development Disease 40 0.043
178
HMN016 Hemangioendothelioma 40 0.043
179
c INV001 Invasive Aspergillosis 44 0.043
180
IMM127 Immune System Cancer 41 0.043
181
P MSN006 Mesenchymoma 31 0.043
182
THL010 Thalassemia Minor 38 0.043
183
CNG069 Congenital Cytomegalovirus 34 0.043
184
FBR002 Fibrosarcoma of Bone 41 0.043
185
BNS002 Bone Structure Disease 37 0.043
186
LYM095 Lymphangiomatosis 32 0.043
187
RDT014 Radiation Myelitis 17 0.043
188
SVR077 Severe Combined Immune Deficiency 36 0.043
189
VSC047 Vascular Malformation 45 0.043
190
OST097 Osteoporotic Fracture 25 0.043