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

203 hits were found for 'hematopoiesis'

# ++ Fam MCID Name MIFTS Score
1
CYC004 Cyclic Hematopoiesis 45 5.473
2
LKM002 Leukemia 70 0.290
3
IDP044 Idiopathic Pulmonary Alveolar Proteinosis 47 0.183
4
THL005 Thalassemia 69 0.173
5
P MYL005 Myelofibrosis 67 0.168
6
APL001 Aplastic Anemia 77 0.162
7
ACT073 Acute Leukemia 62 0.157
8
IDP042 Idiopathic Recurrent Stupor 15 0.157
9
MYL006 Myeloid Leukemia 64 0.151
10
PRX003 Paroxysmal Nocturnal Hemoglobinuria 55 0.151
11
HMG002 Hemoglobinuria 52 0.151
12
SPS077 Sepsis 67 0.145
13
P HRD011 Hereditary Spherocytosis 59 0.133
14
P STR035 Streptococcal Group a Invasive Disease 15 0.133
15
BTT002 Beta Thalassemia 69 0.126
16
DDF001 Dedifferentiated Liposarcoma 48 0.119
17
ACT019 Acute Myeloid Leukemia 87 0.111
18
PLY001 Polycythemia Vera 77 0.111
19
c MYL014 Myeloproliferative Disorder 54 0.111
20
PLY018 Polycythemia 55 0.103
21
RFR010 Refractory Anemia 50 0.103
22
c ALM001 Al Amyloidosis 49 0.103
23
LKP003 Leukoplakia 45 0.103
24
CHR286 Chronic Neutrophilic Leukemia 42 0.103
25
ANK002 Ankylosing Spondylitis 75 0.094
26
MYL040 Myelodysplastic Syndromes 72 0.094
27
P OST001 Osteopetrosis 59 0.094
28
TCL004 T-Cell Leukemia 50 0.094
29
ZYG002 Zygomycosis 38 0.094
30
HMG021 Hemoglobin E - Beta-Thalassemia 34 0.094
31
P BRS047 Breast Cancer 85 0.084
32
ATX002 Ataxia Telangiectasia 81 0.084
33
P HYP075 Hypertension 76 0.084
34
CHR065 Chronic Myeloid Leukemia 67 0.084
35
c NTR004 Neutropenia 59 0.084
36
P PNC001 Pancytopenia 55 0.084
37
SCN006 Secondary Syphilis 53 0.084
38
SPL018 Splenomegaly 50 0.084
39
c CPL003 Capillary Leak Syndrome 44 0.084
40
THR013 Thoracic Outlet Syndrome 53 0.073
41
PYG006 Pyogenic Granuloma 52 0.073
42
LKM001 Leukemoid Reaction 44 0.073
43
HMT018 Hematopoietic Stem Cell Transplantation 41 0.073
44
CNG003 Congenital Dyserythropoietic Anemia 41 0.073
45
HMG003 Hemoglobin E Disease 40 0.073
46
ENT001 Enterocele 39 0.073
47
RTC003 Root Caries 35 0.073
48
HMG004 Hemoglobin D Disease 24 0.073
49
CRH001 Crohn's Disease 78 0.059
50
SVR004 Severe Combined Immunodeficiency 75 0.059
51
BRN024 Bronchitis 71 0.059
52
ACN002 Acanthosis Nigricans 70 0.059
53
c THR014 Thrombocytopenia 66 0.059
54
CHD001 Chediak-Higashi Syndrome 66 0.059
55
CLN016 Colon Cancer 66 0.059
56
RLP001 Relapsing Polychondritis 66 0.059
57
P GRF002 Graft Versus Host Disease 64 0.059
58
THR004 Thrombocytosis 61 0.059
59
P HYP098 Hypereosinophilic Syndrome 61 0.059
60
c ESS003 Essential Thrombocythemia 60 0.059
61
P ADN016 Adenocarcinoma 60 0.059
62
MYC002 Mycobacterium Avium Complex Disease 56 0.059
63
HPT022 Hepatoblastoma 56 0.059
64
FLT001 Felty's Syndrome 54 0.059
65
PYR013 Pyruvate Kinase Deficiency 54 0.059
66
CHR285 Chronic Myelomonocytic Leukemia 53 0.059
67
HYP063 Hypersplenism 52 0.059
68
PRN011 Pernicious Anemia 52 0.059
69
MNC007 Monocytic Leukemia 51 0.059
70
c WLM002 Wilms Tumor 50 0.059
71
CYT008 Cytomegalovirus Infection 50 0.059
72
HMN009 Hemangioblastoma 50 0.059
73
P PND001 Pain Disorder 49 0.059
74
P THR090 Thrombocythemia 1 48 0.059
75
c OST019 Osteosclerosis 48 0.059
76
SDR003 Sideroblastic Anemia 44 0.059
77
PRP016 Paraplegia 42 0.059
78
MCR017 Macrocytic Anemia 40 0.059
79
STC004 Stachybotrys Chartarum 39 0.059
80
PNC033 Pancreas Adenocarcinoma 39 0.059
81
BNM001 Bone Marrow Cancer 38 0.059
82
MYL046 Myelodysplastic Syndrome, Somatic 32 0.059
83
NNS006 Non-Suppurative Otitis Media 24 0.059
84
PHL007 Philadelphia-Negative Chronic Myeloid Leukemia 23 0.059
85
HMG022 Hemoglobin C - Beta-Thalassemia 19 0.059
86
P AMY001 Amyotrophic Lateral Sclerosis 87 0.042
87
P RHM011 Rheumatoid Arthritis 83 0.042
88
TBR010 Tuberculosis 82 0.042
89
P MLT019 Multiple Myeloma 76 0.042
90
P ART022 Arthritis 75 0.042
91
AND002 Androgen Insensitivity Syndrome 75 0.042
92
P FML018 Familial Mediterranean Fever 73 0.042
93
P GCH001 Gaucher's Disease 73 0.042
94
P AST007 Astrocytoma 70 0.042
95
ATH003 Atherosclerosis 69 0.042
96
P CNG006 Congenital Hypothyroidism 69 0.042
97
P CRN008 Carney Complex 68 0.042
98
ALP006 Alpha Thalassemia 68 0.042
99
ASP006 Aspergillosis 68 0.042
100
P MNN012 Meningioma 67 0.042
101
ADN018 Adenoma 67 0.042
102
P ANG001 Angelman Syndrome 67 0.042
103
DFC004 Deficiency Anemia 65 0.042
104
P PRT013 Portal Hypertension 65 0.042
105
c HYP095 Hypercholesterolemia 65 0.042
106
ART019 Aortic Valve Stenosis 64 0.042
107
PRC016 Pre-Eclampsia 64 0.042
108
WST001 West Syndrome 64 0.042
109
LNG024 Langerhans-Cell Histiocytosis 63 0.042
110
ECL001 Eclampsia 62 0.042
111
HMN010 Hemangioma 62 0.042
112
P HLP001 Holoprosencephaly 61 0.042
113
HYD012 Hydrops Fetalis 61 0.042
114
DMN001 Diamond-Blackfan Anemia 61 0.042
115
P HST010 Histiocytosis 61 0.042
116
PRP001 Propionic Acidemia 60 0.042
117
TYP007 Typhoid Fever 60 0.042
118
ACT020 Acute T Cell Leukemia 59 0.042
119
P DWR001 Dwarfism 59 0.042
120
ACT117 Acute Myelomonocytic Leukemia 58 0.042
121
c PNC044 Pancreatitis 58 0.042
122
c AXN002 Axenfeld-Rieger Syndrome 57 0.042
123
c ATX004 Ataxia 56 0.042
124
CMP002 Campylobacteriosis 56 0.042
125
LST001 Listeriosis 56 0.042
126
P FBR017 Fibrosarcoma 56 0.042
127
c EMR001 Emery-Dreifuss Muscular Dystrophy 56 0.042
128
SLT008 Solitary Fibrous Tumor 55 0.042
129
P SVR003 Severe Congenital Neutropenia 55 0.042
130
THY022 Thymic Carcinoma 55 0.042
131
ERY009 Erythropoietic Protoporphyria 55 0.042
132
P PLM006 Pulmonary Alveolar Proteinosis 55 0.042
133
APP008 Appendicitis 54 0.042
134
DPH001 Diphtheria 54 0.042
135
SRC014 Sarcoma 54 0.042
136
P ESN007 Eosinophilia 54 0.042
137
c MYL007 Myeloma 53 0.042
138
P CNT005 Central Nervous System Lymphoma 53 0.042
139
CHR005 Chorioamnionitis 52 0.042
140
c KDN018 Kidney Disease 52 0.042
141
PLS011 Plasmacytoma 52 0.042
142
EXT010 Extramedullary Plasmacytoma 52 0.042
143
ART001 Arterial Tortuosity Syndrome 52 0.042
144
NTR003 Natural Killer Cell Leukemia 52 0.042
145
c GGN002 Gigantism 51 0.042
146
EPT020 Epithelioid Hemangioendothelioma 51 0.042
147
HMS001 Hemosiderosis 51 0.042
148
GRY002 Gray Platelet Syndrome 51 0.042
149
IDP064 Idiopathic Neutropenia 51 0.042
150
MYL001 Myelitis 51 0.042
151
HMN016 Hemangioendothelioma 51 0.042
152
P PLC011 Pilocytic Astrocytoma 51 0.042
153
ADL002 Adult Syndrome 50 0.042
154
LYM026 Lymphoblastic Leukemia 49 0.042
155
ACT100 Acute Febrile Neutrophilic Dermatosis 49 0.042
156
NDL013 Nodular Regenerative Hyperplasia 49 0.042
157
c CTR002 Cataract 48 0.042
158
P CHR092 Chronic Myeloproliferative Disease 48 0.042
159
NTR021 Nutrition Disease 48 0.042
160
PNM008 Pneumothorax 48 0.042
161
P END047 Endophthalmitis 48 0.042
162
MCN007 Meconium Aspiration Syndrome 47 0.042
163
INV001 Invasive Aspergillosis 47 0.042
164
c ENC008 Encephalocele 47 0.042
165
DNT012 Dental Caries 46 0.042
166
LKP004 Leukopenia 46 0.042
167
P CNG052 Congenital Amegakaryocytic Thrombocytopenia 45 0.042
168
THY035 Thyroid Adenoma 44 0.042
169
c SPN183 Spontaneous Pneumothorax 44 0.042
170
RCR001 Recurrent Corneal Erosion 43 0.042
171
FLL031 Follicular Adenoma 43 0.042
172
HST016 Histiocytic Sarcoma 43 0.042
173
CHR101 Char Syndrome 42 0.042
174
CNG045 Congenital Dyserythropoietic Anemia Type I 41 0.042
175
GRN017 Granulocytopenia 41 0.042
176
c OPT004 Optic Atrophy 41 0.042
177
AND003 Andersen-Tawil Syndrome 39 0.042
178
P OST051 Osteopetrosis Autosomal Recessive 1 38 0.042
179
c MSN006 Mesenchymoma 36 0.042
180
BNM005 Bone Marrow Necrosis 35 0.042
181
VRL011 Viral Infectious Disease 35 0.042
182
EMN001 Emanuel Syndrome 34 0.042
183
c ATX010 Ataxia Neuropathy Spectrum 33 0.042
184
CNG069 Congenital Cytomegalovirus 33 0.042
185
ENM001 Enamel Caries 31 0.042
186
MCR029 Micro Syndrome 31 0.042
187
P SLP004 Salpingo-Oophoritis 30 0.042
188
HMG015 Hemoglobin S Beta-Thalassemia 30 0.042
189
LVR014 Liver Sarcoma 29 0.042
190
HMG001 Hemoglobin C Disease 28 0.042
191
HMR001 Hemorrhagic Thrombocythemia 28 0.042
192
BNZ002 Benzene Toxicity 28 0.042
193
SPL012 Splenic Disease 26 0.042
194
c BNG012 Benign Mesenchymoma 20 0.042
195
DFF022 Diffuse Neonatal Hemangiomatosis 20 0.042
196
AND005 Androgen Insensitivity Syndrome, Mild 19 0.042
197
c BNG076 Benign Exophthalmos Syndrome 17 0.042
198
CHR079 Choroid Disease 16 0.042
199
PRS024 Parasagittal Meningioma 15 0.042
200
BNR001 Bone Remodeling Disease 13 0.042
201
RDT014 Radiation Myelitis 13 0.042
202
c NTR033 Neutropenia, Severe Congenital 1, Autosomal Dominant 12 0.042
203
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 5 0.042