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

175 hits were found for 'hematopoiesis'

# Family MCID Name MIFTS Score
1
CYC004 Cyclic Hematopoiesis 52 5.503
2
P LKM002 Leukemia 79 0.306
3
IDP044 Idiopathic Pulmonary Alveolar Proteinosis 44 0.192
4
c THL005 Thalassemia 68 0.182
5
P MYL005 Myelofibrosis 75 0.176
6
P APL001 Aplastic Anemia 83 0.171
7
c ACT073 Acute Leukemia 62 0.165
8
IDP042 Idiopathic Recurrent Stupor 15 0.165
9
c MYL006 Myeloid Leukemia 72 0.159
10
HMG002 Hemoglobinuria 55 0.159
11
SPS077 Sepsis 58 0.146
12
P HRD011 Hereditary Spherocytosis 66 0.139
13
P STR035 Streptococcal Group a Invasive Disease 14 0.139
14
c BTT002 Beta Thalassemia 70 0.132
15
DDF001 Dedifferentiated Liposarcoma 42 0.125
16
P ACT019 Acute Myeloid Leukemia 94 0.117
17
PLY001 Polycythemia Vera 83 0.117
18
c PLY018 Polycythemia 61 0.108
19
c ALM001 Al Amyloidosis 44 0.108
20
CHR286 Chronic Neutrophilic Leukemia 38 0.108
21
LKP003 Leukoplakia 32 0.108
22
ANK002 Ankylosing Spondylitis 75 0.099
23
P OST001 Osteopetrosis 60 0.099
24
ZYG002 Zygomycosis 28 0.099
25
P BRS047 Breast Cancer 105 0.088
26
P ATX002 Ataxia Telangiectasia 93 0.088
27
P HYP075 Hypertension 86 0.088
28
c CHR065 Chronic Myeloid Leukemia 74 0.088
29
c NTR004 Neutropenia 65 0.088
30
MDS022 Mediastinitis 56 0.088
31
P PNC001 Pancytopenia 55 0.088
32
SCN006 Secondary Syphilis 55 0.088
33
c TCL004 T-Cell Leukemia 49 0.088
34
c CPL003 Capillary Leak Syndrome 47 0.088
35
THR013 Thoracic Outlet Syndrome 54 0.076
36
LKM001 Leukemoid Reaction 45 0.076
37
c CNG003 Congenital Dyserythropoietic Anemia 44 0.076
38
ENT001 Enterocele 42 0.076
39
P HMG003 Hemoglobin E Disease 42 0.076
40
RTC003 Root Caries 36 0.076
41
SVR004 Severe Combined Immunodeficiency 85 0.062
42
CRH001 Crohn's Disease 83 0.062
43
BRN024 Bronchitis 76 0.062
44
CHD001 Chediak-Higashi Syndrome 74 0.062
45
ACN002 Acanthosis Nigricans 73 0.062
46
RLP001 Relapsing Polychondritis 69 0.062
47
c THR014 Thrombocytopenia 67 0.062
48
c PNC044 Pancreatitis 67 0.062
49
DFC004 Deficiency Anemia 66 0.062
50
HPT022 Hepatoblastoma 65 0.062
51
P GRF002 Graft Versus Host Disease 65 0.062
52
THR004 Thrombocytosis 63 0.062
53
FLT001 Felty's Syndrome 62 0.062
54
HMN009 Hemangioblastoma 60 0.062
55
P ADN016 Adenocarcinoma 60 0.062
56
c MNC007 Monocytic Leukemia 59 0.062
57
MYC002 Mycobacterium Avium Complex Disease 57 0.062
58
OST019 Osteosclerosis 56 0.062
59
HYP063 Hypersplenism 56 0.062
60
P THR090 Thrombocythemia 1 54 0.062
61
PRN011 Pernicious Anemia 52 0.062
62
P PND001 Pain Disorder 49 0.062
63
P SDR003 Sideroblastic Anemia 48 0.062
64
PRP016 Paraplegia 48 0.062
65
PNC033 Pancreas Adenocarcinoma 46 0.062
66
MCR017 Macrocytic Anemia 44 0.062
67
MYL046 Myelodysplastic Syndrome, Somatic 36 0.062
68
STC004 Stachybotrys Chartarum 32 0.062
69
NNS006 Non-Suppurative Otitis Media 26 0.062
70
P AMY001 Amyotrophic Lateral Sclerosis 100 0.044
71
P OBS005 Obesity 93 0.044
72
P RHM011 Rheumatoid Arthritis 91 0.044
73
P MLT019 Multiple Myeloma 89 0.044
74
AND002 Androgen Insensitivity Syndrome 88 0.044
75
TBR010 Tuberculosis 84 0.044
76
P MNN012 Meningioma 79 0.044
77
P GCH001 Gaucher's Disease 79 0.044
78
PRT036 Peritonitis 78 0.044
79
P CRN008 Carney Complex 78 0.044
80
LNG024 Langerhans-Cell Histiocytosis 75 0.044
81
P ART022 Arthritis 75 0.044
82
PRC016 Pre-Eclampsia 75 0.044
83
c HPT021 Hepatitis 75 0.044
84
P ALP006 Alpha Thalassemia 75 0.044
85
P FML018 Familial Mediterranean Fever 74 0.044
86
ASP006 Aspergillosis 73 0.044
87
P AST007 Astrocytoma 72 0.044
88
c CNG006 Congenital Hypothyroidism 72 0.044
89
P HST010 Histiocytosis 71 0.044
90
c MNN013 Meningitis 71 0.044
91
ATH003 Atherosclerosis 71 0.044
92
P ANG001 Angelman Syndrome 70 0.044
93
P PRP001 Propionic Acidemia 69 0.044
94
ART019 Aortic Valve Stenosis 68 0.044
95
ADN018 Adenoma 67 0.044
96
c THY032 Thyroiditis 67 0.044
97
P PRT013 Portal Hypertension 67 0.044
98
P FBR017 Fibrosarcoma 66 0.044
99
WST001 West Syndrome 64 0.044
100
XLN006 X-Linked Sideroblastic Anemia 64 0.044
101
MYL040 Myelodysplastic Syndromes 64 0.044
102
ECL001 Eclampsia 63 0.044
103
PLS011 Plasmacytoma 63 0.044
104
TYP007 Typhoid Fever 63 0.044
105
SRC014 Sarcoma 63 0.044
106
LST001 Listeriosis 62 0.044
107
ART001 Arterial Tortuosity Syndrome 62 0.044
108
DWN001 Down Syndrome 62 0.044
109
c DMN001 Diamond-Blackfan Anemia 61 0.044
110
P HLP001 Holoprosencephaly 61 0.044
111
P ESN007 Eosinophilia 60 0.044
112
c AXN002 Axenfeld-Rieger Syndrome 60 0.044
113
P ESP024 Esophagitis 60 0.044
114
c MYL007 Myeloma 59 0.044
115
DPH001 Diphtheria 59 0.044
116
P SVR003 Severe Congenital Neutropenia 59 0.044
117
CMP002 Campylobacteriosis 59 0.044
118
P DWR001 Dwarfism 58 0.044
119
c KDN018 Kidney Disease 58 0.044
120
APP008 Appendicitis 57 0.044
121
CHR008 Choroiditis 57 0.044
122
c HPT015 Hepatitis D 57 0.044
123
P LYM026 Lymphoblastic Leukemia 56 0.044
124
P PLM006 Pulmonary Alveolar Proteinosis 56 0.044
125
P END047 Endophthalmitis 56 0.044
126
NTR003 Natural Killer Cell Leukemia 56 0.044
127
ERY009 Erythropoietic Protoporphyria 56 0.044
128
P CNT005 Central Nervous System Lymphoma 56 0.044
129
CHR005 Chorioamnionitis 56 0.044
130
PNM008 Pneumothorax 55 0.044
131
EXT010 Extramedullary Plasmacytoma 55 0.044
132
P CHR092 Chronic Myeloproliferative Disease 55 0.044
133
P HYP098 Hypereosinophilic Syndrome 54 0.044
134
PRR002 Pure Red-Cell Aplasia 54 0.044
135
c CTR002 Cataract 53 0.044
136
c ADL017 Adult T-Cell Leukemia 53 0.044
137
ADL002 Adult Syndrome 52 0.044
138
MCN007 Meconium Aspiration Syndrome 52 0.044
139
MYL001 Myelitis 52 0.044
140
HMS001 Hemosiderosis 52 0.044
141
DNT012 Dental Caries 51 0.044
142
c ACT117 Acute Myelomonocytic Leukemia 51 0.044
143
THY022 Thymic Carcinoma 51 0.044
144
IDP064 Idiopathic Neutropenia 50 0.044
145
FLL031 Follicular Adenoma 49 0.044
146
INV001 Invasive Aspergillosis 49 0.044
147
c OPT004 Optic Atrophy 46 0.044
148
P OST051 Osteopetrosis Autosomal Recessive 1 46 0.044
149
c CHR285 Chronic Myelomonocytic Leukemia 46 0.044
150
RCR001 Recurrent Corneal Erosion 44 0.044
151
P ATX010 Ataxia Neuropathy Spectrum 44 0.044
152
ACT100 Acute Febrile Neutrophilic Dermatosis 43 0.044
153
AND003 Andersen-Tawil Syndrome 43 0.044
154
c MSN006 Mesenchymoma 42 0.044
155
SYN053 Syndromic Diarrhea 42 0.044
156
FBR002 Fibrosarcoma of Bone 39 0.044
157
XLN003 X-Linked Sideroblastic Anemia with Ataxia 38 0.044
158
LVR014 Liver Sarcoma 37 0.044
159
VRL011 Viral Infectious Disease 37 0.044
160
EMN001 Emanuel Syndrome 36 0.044
161
HMR001 Hemorrhagic Thrombocythemia 34 0.044
162
LKP004 Leukopenia 33 0.044
163
ENM001 Enamel Caries 32 0.044
164
P SLP004 Salpingo-Oophoritis 31 0.044
165
GRN017 Granulocytopenia 31 0.044
166
SPL012 Splenic Disease 29 0.044
167
CHR079 Choroid Disease 21 0.044
168
c BNG076 Benign Exophthalmos Syndrome 21 0.044
169
c BNG012 Benign Mesenchymoma 20 0.044
170
c NTR033 Neutropenia, Severe Congenital 1, Autosomal Dominant 19 0.044
171
AND005 Androgen Insensitivity Syndrome, Mild 18 0.044
172
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 18 0.044
173
PRT025 Protein-Deficiency Anemia 17 0.044
174
BNR001 Bone Remodeling Disease 17 0.044
175
PRS024 Parasagittal Meningioma 15 0.044