Search results for "hematopoiesis"

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

188 hits were found for 'hematopoiesis'

# Family MCID Name MIFTS Score
1
CYC004 Cyclic Hematopoiesis 54 5.486
2
P LKM002 Leukemia 77 0.299
3
P MYL005 Myelofibrosis 75 0.188
4
c THL005 Thalassemia 72 0.178
5
P APL001 Aplastic Anemia 83 0.173
6
MYL040 Myelodysplastic Syndromes 81 0.156
7
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 54 0.156
8
HMG002 Hemoglobinuria 52 0.156
9
c MYL006 Myeloid Leukemia 75 0.150
10
P HRD011 Hereditary Spherocytosis 67 0.137
11
c BTT002 Beta Thalassemia 78 0.122
12
P ACT019 Acute Myeloid Leukemia 93 0.114
13
PLY001 Polycythemia Vera 85 0.114
14
c PLY018 Polycythemia 59 0.106
15
END072 Endotheliitis 51 0.106
16
P OST001 Osteopetrosis 66 0.097
17
P HYP075 Hypertension 87 0.086
18
P BRS047 Breast Cancer 86 0.086
19
c CHR065 Chronic Myeloid Leukemia 73 0.086
20
c NTR004 Neutropenia 64 0.086
21
SPL018 Splenomegaly 47 0.086
22
MDS022 Mediastinitis 46 0.086
23
HMT018 Hematopoietic Stem Cell Transplantation 41 0.086
24
PYG006 Pyogenic Granuloma 50 0.075
25
P PNC001 Pancytopenia 48 0.075
26
P HMG003 Hemoglobin E Disease 45 0.075
27
c CNG003 Congenital Dyserythropoietic Anemia 43 0.075
28
CHD001 Chediak-Higashi Syndrome 76 0.061
29
c THR014 Thrombocytopenia 71 0.061
30
SPS077 Sepsis 70 0.061
31
c PNC044 Pancreatitis 69 0.061
32
PYR013 Pyruvate Kinase Deficiency 67 0.061
33
P WLM002 Wilms Tumor 66 0.061
34
P GRF002 Graft Versus Host Disease 65 0.061
35
HV1006 Hiv-1 64 0.061
36
HPT022 Hepatoblastoma 62 0.061
37
c ESS003 Essential Thrombocythemia 61 0.061
38
THR004 Thrombocytosis 61 0.061
39
P ADN016 Adenocarcinoma 59 0.061
40
c MNC007 Monocytic Leukemia 57 0.061
41
c ACT073 Acute Leukemia 57 0.061
42
HMN009 Hemangioblastoma 55 0.061
43
PRN011 Pernicious Anemia 53 0.061
44
OST019 Osteosclerosis 52 0.061
45
c TCL004 T-Cell Leukemia 51 0.061
46
RFR010 Refractory Anemia 50 0.061
47
PRP016 Paraplegia 48 0.061
48
MCR017 Macrocytic Anemia 45 0.061
49
P SDR003 Sideroblastic Anemia 44 0.061
50
CYT008 Cytomegalovirus Infection 44 0.061
51
P HMG021 Hemoglobin E - Beta-Thalassemia 27 0.061
52
MN1001 Mn1 21 0.061
53
P RHM011 Rheumatoid Arthritis 94 0.043
54
P OBS005 Obesity 91 0.043
55
P MLT019 Multiple Myeloma 88 0.043
56
P ATX002 Ataxia Telangiectasia 87 0.043
57
TBR010 Tuberculosis 87 0.043
58
P GCH001 Gaucher's Disease 84 0.043
59
AND002 Androgen Insensitivity Syndrome 80 0.043
60
P PRC016 Pre-Eclampsia 78 0.043
61
P MNN012 Meningioma 78 0.043
62
ANK002 Ankylosing Spondylitis 77 0.043
63
CRH001 Crohn's Disease 76 0.043
64
P FML018 Familial Mediterranean Fever 76 0.043
65
P ART022 Arthritis 75 0.043
66
P ALP006 Alpha Thalassemia 75 0.043
67
SVR004 Severe Combined Immunodeficiency 74 0.043
68
P AST007 Astrocytoma 74 0.043
69
ASP006 Aspergillosis 73 0.043
70
c PLM037 Pulmonary Hypertension 73 0.043
71
c HYP095 Hypercholesterolemia 73 0.043
72
PRT036 Peritonitis 72 0.043
73
P PRP001 Propionic Acidemia 71 0.043
74
P ANG001 Angelman Syndrome 70 0.043
75
P RTH001 Rothmund-Thomson Syndrome 70 0.043
76
SRC014 Sarcoma 70 0.043
77
ATH003 Atherosclerosis 69 0.043
78
c MNN013 Meningitis 68 0.043
79
c AXN002 Axenfeld-Rieger Syndrome 67 0.043
80
P CRN008 Carney Complex 67 0.043
81
c AMY001 Amyotrophic Lateral Sclerosis 67 0.043
82
c THY032 Thyroiditis 66 0.043
83
ADN018 Adenoma 66 0.043
84
c ECL001 Eclampsia 64 0.043
85
ART019 Aortic Valve Stenosis 64 0.043
86
c HPT021 Hepatitis 64 0.043
87
XLN006 X-Linked Sideroblastic Anemia 64 0.043
88
c HLP001 Holoprosencephaly 64 0.043
89
c CNG006 Congenital Hypothyroidism 64 0.043
90
FLT001 Felty's Syndrome 64 0.043
91
P ESP024 Esophagitis 64 0.043
92
P HST010 Histiocytosis 64 0.043
93
P FBR017 Fibrosarcoma 63 0.043
94
CMP002 Campylobacteriosis 63 0.043
95
ACN002 Acanthosis Nigricans 63 0.043
96
c INT070 Intestinal Obstruction 63 0.043
97
GRY002 Gray Platelet Syndrome 63 0.043
98
c KDN018 Kidney Disease 63 0.043
99
P ESN007 Eosinophilia 63 0.043
100
P ACT101 Acute Lymphoblastic Leukemia 63 0.043
101
c DMN001 Diamond-Blackfan Anemia 62 0.043
102
TYP007 Typhoid Fever 62 0.043
103
HYD012 Hydrops Fetalis 62 0.043
104
P HYP098 Hypereosinophilic Syndrome 62 0.043
105
ERY009 Erythropoietic Protoporphyria 62 0.043
106
DWN001 Down Syndrome 62 0.043
107
c MYL007 Myeloma 61 0.043
108
IDP064 Idiopathic Neutropenia 61 0.043
109
c ALM001 Al Amyloidosis 61 0.043
110
c AMY077 Amyotrophic Lateral Sclerosis Type 18 60 0.043
111
P END047 Endophthalmitis 60 0.043
112
MYC002 Mycobacterium Avium Complex Disease 59 0.043
113
HYP063 Hypersplenism 59 0.043
114
EXT010 Extramedullary Plasmacytoma 59 0.043
115
c ATX004 Ataxia 59 0.043
116
DPH001 Diphtheria 58 0.043
117
LST001 Listeriosis 58 0.043
118
EPT020 Epithelioid Hemangioendothelioma 58 0.043
119
HMS001 Hemosiderosis 57 0.043
120
MCN007 Meconium Aspiration Syndrome 57 0.043
121
PLS011 Plasmacytoma 57 0.043
122
NTR003 Natural Killer Cell Leukemia 57 0.043
123
P PLC011 Pilocytic Astrocytoma 57 0.043
124
c CTR002 Cataract 57 0.043
125
LNG024 Langerhans-Cell Histiocytosis 57 0.043
126
NDL013 Nodular Regenerative Hyperplasia 57 0.043
127
c LYM026 Lymphoblastic Leukemia 57 0.043
128
ACT100 Acute Febrile Neutrophilic Dermatosis 57 0.043
129
P AMY074 Amyotrophic Lateral Sclerosis Type 14 56 0.043
130
APP008 Appendicitis 56 0.043
131
P CNG052 Congenital Amegakaryocytic Thrombocytopenia 56 0.043
132
PRR002 Pure Red-Cell Aplasia 56 0.043
133
c CHR285 Chronic Myelomonocytic Leukemia 56 0.043
134
HRD024 Hereditary Persistence of Fetal Hemoglobin 55 0.043
135
P DWR001 Dwarfism 55 0.043
136
ART001 Arterial Tortuosity Syndrome 55 0.043
137
SLT008 Solitary Fibrous Tumor 55 0.043
138
MYL001 Myelitis 55 0.043
139
CHR008 Choroiditis 54 0.043
140
AND003 Andersen-Tawil Syndrome 54 0.043
141
P ENC008 Encephalocele 54 0.043
142
P PLM006 Pulmonary Alveolar Proteinosis 53 0.043
143
IDP044 Idiopathic Pulmonary Alveolar Proteinosis 53 0.043
144
P CNT005 Central Nervous System Lymphoma 53 0.043
145
INV001 Invasive Aspergillosis 53 0.043
146
c CPL003 Capillary Leak Syndrome 53 0.043
147
c SPN183 Spontaneous Pneumothorax 52 0.043
148
THR013 Thoracic Outlet Syndrome 52 0.043
149
HST016 Histiocytic Sarcoma 52 0.043
150
P PND001 Pain Disorder 52 0.043
151
CHR005 Chorioamnionitis 50 0.043
152
P CHR092 Chronic Myeloproliferative Disease 50 0.043
153
PNM008 Pneumothorax 50 0.043
154
c OPT004 Optic Atrophy 50 0.043
155
THY022 Thymic Carcinoma 49 0.043
156
LKM001 Leukemoid Reaction 49 0.043
157
CHR286 Chronic Neutrophilic Leukemia 49 0.043
158
PNC033 Pancreas Adenocarcinoma 49 0.043
159
c GGN002 Gigantism 48 0.043
160
FLL031 Follicular Adenoma 48 0.043
161
GRN017 Granulocytopenia 47 0.043
162
STC004 Stachybotrys Chartarum 46 0.043
163
c ADL017 Adult T-Cell Leukemia 46 0.043
164
LKP003 Leukoplakia 46 0.043
165
HMN016 Hemangioendothelioma 46 0.043
166
BNF002 Bone Fracture 45 0.043
167
ZYG002 Zygomycosis 45 0.043
168
P ATX010 Ataxia Neuropathy Spectrum 43 0.043
169
c MSN006 Mesenchymoma 42 0.043
170
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.043
171
FBR002 Fibrosarcoma of Bone 42 0.043
172
c HMN021 Human T-Cell Leukemia Virus Type 1 41 0.043
173
c CHR253 Chromosome 5q Deletion 40 0.043
174
VRL011 Viral Infectious Disease 39 0.043
175
CNG069 Congenital Cytomegalovirus 36 0.043
176
XLN003 X-Linked Sideroblastic Anemia with Ataxia 35 0.043
177
HMR001 Hemorrhagic Thrombocythemia 35 0.043
178
SYN053 Syndromic Diarrhea 34 0.043
179
c OST051 Osteopetrosis Autosomal Recessive 1 26 0.043
180
DFF022 Diffuse Neonatal Hemangiomatosis 25 0.043
181
c BNG012 Benign Mesenchymoma 23 0.043
182
c BNG076 Benign Exophthalmos Syndrome 22 0.043
183
AND005 Androgen Insensitivity Syndrome, Mild 21 0.043
184
MYL046 Myelodysplastic Syndrome, Somatic 20 0.043
185
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 18 0.043
186
PRS024 Parasagittal Meningioma 17 0.043
187
RDT014 Radiation Myelitis 16 0.043
188
c NTR033 Neutropenia, Severe Congenital 1, Autosomal Dominant 16 0.043