Search results for "hematopoiesis"

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

181 hits were found for 'hematopoiesis'

# Family MCID Name MIFTS Score
1
CYC004 Cyclic Hematopoiesis 52 5.489
2
P LKM002 Leukemia 77 0.300
3
c THL005 Thalassemia 72 0.180
4
P MYL005 Myelofibrosis 72 0.175
5
P APL001 Aplastic Anemia 82 0.169
6
MYL040 Myelodysplastic Syndromes 79 0.158
7
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 56 0.158
8
HMG002 Hemoglobinuria 52 0.158
9
c MYL006 Myeloid Leukemia 72 0.151
10
P HRD011 Hereditary Spherocytosis 62 0.138
11
c BTT002 Beta Thalassemia 77 0.124
12
P ACT019 Acute Myeloid Leukemia 92 0.116
13
PLY001 Polycythemia Vera 82 0.116
14
c MYL014 Myeloproliferative Disorder 52 0.116
15
c PLY018 Polycythemia 61 0.107
16
END072 Endotheliitis 50 0.107
17
P OST001 Osteopetrosis 63 0.098
18
P BRS047 Breast Cancer 100 0.087
19
P HYP075 Hypertension 85 0.087
20
c CHR065 Chronic Myeloid Leukemia 71 0.087
21
c NTR004 Neutropenia 64 0.087
22
SPL018 Splenomegaly 46 0.087
23
MDS022 Mediastinitis 46 0.087
24
HMT018 Hematopoietic Stem Cell Transplantation 40 0.087
25
PYG006 Pyogenic Granuloma 49 0.076
26
P PNC001 Pancytopenia 48 0.076
27
P HMG003 Hemoglobin E Disease 45 0.076
28
c CNG003 Congenital Dyserythropoietic Anemia 41 0.076
29
SVR004 Severe Combined Immunodeficiency 80 0.062
30
CHD001 Chediak-Higashi Syndrome 75 0.062
31
SPS077 Sepsis 70 0.062
32
c THR014 Thrombocytopenia 70 0.062
33
c PNC044 Pancreatitis 69 0.062
34
PYR013 Pyruvate Kinase Deficiency 65 0.062
35
HPT022 Hepatoblastoma 62 0.062
36
HV1006 Hiv-1 61 0.062
37
P GRF002 Graft Versus Host Disease 60 0.062
38
THR004 Thrombocytosis 59 0.062
39
c ESS003 Essential Thrombocythemia 59 0.062
40
c MNC007 Monocytic Leukemia 58 0.062
41
P ADN016 Adenocarcinoma 58 0.062
42
c ACT073 Acute Leukemia 56 0.062
43
HMN009 Hemangioblastoma 54 0.062
44
PRN011 Pernicious Anemia 53 0.062
45
c WLM002 Wilms Tumor 51 0.062
46
OST019 Osteosclerosis 51 0.062
47
c TCL004 T-Cell Leukemia 50 0.062
48
RFR010 Refractory Anemia 48 0.062
49
PRP016 Paraplegia 47 0.062
50
MCR017 Macrocytic Anemia 45 0.062
51
P SDR003 Sideroblastic Anemia 44 0.062
52
CYT008 Cytomegalovirus Infection 43 0.062
53
MYL046 Myelodysplastic Syndrome, Somatic 36 0.062
54
P HMG021 Hemoglobin E - Beta-Thalassemia 25 0.062
55
P AMY001 Amyotrophic Lateral Sclerosis 98 0.044
56
P RHM011 Rheumatoid Arthritis 93 0.044
57
P OBS005 Obesity 89 0.044
58
P ATX002 Ataxia Telangiectasia 86 0.044
59
TBR010 Tuberculosis 83 0.044
60
P MLT019 Multiple Myeloma 82 0.044
61
AND002 Androgen Insensitivity Syndrome 80 0.044
62
P MNN012 Meningioma 78 0.044
63
P GCH001 Gaucher's Disease 77 0.044
64
P ART022 Arthritis 75 0.044
65
P FML018 Familial Mediterranean Fever 74 0.044
66
ANK002 Ankylosing Spondylitis 74 0.044
67
PRC016 Pre-Eclampsia 74 0.044
68
CRH001 Crohn's Disease 74 0.044
69
ASP006 Aspergillosis 72 0.044
70
PRT036 Peritonitis 71 0.044
71
P AST007 Astrocytoma 71 0.044
72
P ANG001 Angelman Syndrome 70 0.044
73
P PRP001 Propionic Acidemia 70 0.044
74
ACN002 Acanthosis Nigricans 69 0.044
75
c CNG006 Congenital Hypothyroidism 69 0.044
76
SRC014 Sarcoma 69 0.044
77
c MNN013 Meningitis 68 0.044
78
c AXN002 Axenfeld-Rieger Syndrome 66 0.044
79
P CRN008 Carney Complex 66 0.044
80
c THY032 Thyroiditis 66 0.044
81
c HPT021 Hepatitis 64 0.044
82
ECL001 Eclampsia 64 0.044
83
P HLP001 Holoprosencephaly 64 0.044
84
ADN018 Adenoma 64 0.044
85
ART019 Aortic Valve Stenosis 64 0.044
86
FLT001 Felty's Syndrome 63 0.044
87
P ESP024 Esophagitis 63 0.044
88
CMP002 Campylobacteriosis 63 0.044
89
P FBR017 Fibrosarcoma 63 0.044
90
XLN006 X-Linked Sideroblastic Anemia 62 0.044
91
P HST010 Histiocytosis 62 0.044
92
c KDN018 Kidney Disease 62 0.044
93
P ESN007 Eosinophilia 61 0.044
94
HYD012 Hydrops Fetalis 61 0.044
95
P HYP098 Hypereosinophilic Syndrome 61 0.044
96
c MYL007 Myeloma 61 0.044
97
DWN001 Down Syndrome 61 0.044
98
ERY009 Erythropoietic Protoporphyria 60 0.044
99
GRY002 Gray Platelet Syndrome 60 0.044
100
TYP007 Typhoid Fever 60 0.044
101
IDP064 Idiopathic Neutropenia 60 0.044
102
c ALM001 Al Amyloidosis 59 0.044
103
P END047 Endophthalmitis 59 0.044
104
c DMN001 Diamond-Blackfan Anemia 59 0.044
105
P ALP006 Alpha Thalassemia 58 0.044
106
MYC002 Mycobacterium Avium Complex Disease 58 0.044
107
HYP063 Hypersplenism 58 0.044
108
EXT010 Extramedullary Plasmacytoma 58 0.044
109
EPT020 Epithelioid Hemangioendothelioma 58 0.044
110
c ATX004 Ataxia 58 0.044
111
DPH001 Diphtheria 58 0.044
112
P PLC011 Pilocytic Astrocytoma 57 0.044
113
LST001 Listeriosis 57 0.044
114
MCN007 Meconium Aspiration Syndrome 57 0.044
115
NTR003 Natural Killer Cell Leukemia 57 0.044
116
PLS011 Plasmacytoma 57 0.044
117
c CTR002 Cataract 57 0.044
118
ACT100 Acute Febrile Neutrophilic Dermatosis 56 0.044
119
NDL013 Nodular Regenerative Hyperplasia 56 0.044
120
LNG024 Langerhans-Cell Histiocytosis 56 0.044
121
c CHR285 Chronic Myelomonocytic Leukemia 56 0.044
122
P CNG052 Congenital Amegakaryocytic Thrombocytopenia 55 0.044
123
APP008 Appendicitis 55 0.044
124
SLT008 Solitary Fibrous Tumor 55 0.044
125
HMS001 Hemosiderosis 55 0.044
126
CHR008 Choroiditis 55 0.044
127
HRD024 Hereditary Persistence of Fetal Hemoglobin 55 0.044
128
P DWR001 Dwarfism 55 0.044
129
c LYM026 Lymphoblastic Leukemia 54 0.044
130
PRR002 Pure Red-Cell Aplasia 54 0.044
131
MYL001 Myelitis 54 0.044
132
ART001 Arterial Tortuosity Syndrome 54 0.044
133
AND003 Andersen-Tawil Syndrome 53 0.044
134
IDP044 Idiopathic Pulmonary Alveolar Proteinosis 53 0.044
135
P PLM006 Pulmonary Alveolar Proteinosis 53 0.044
136
P CNT005 Central Nervous System Lymphoma 52 0.044
137
INV001 Invasive Aspergillosis 52 0.044
138
P ENC008 Encephalocele 52 0.044
139
c CPL003 Capillary Leak Syndrome 52 0.044
140
c SPN183 Spontaneous Pneumothorax 52 0.044
141
THR013 Thoracic Outlet Syndrome 52 0.044
142
HST016 Histiocytic Sarcoma 52 0.044
143
c OPT004 Optic Atrophy 50 0.044
144
P CHR092 Chronic Myeloproliferative Disease 50 0.044
145
CHR005 Chorioamnionitis 50 0.044
146
PNM008 Pneumothorax 49 0.044
147
CHR286 Chronic Neutrophilic Leukemia 49 0.044
148
LKM001 Leukemoid Reaction 49 0.044
149
P PND001 Pain Disorder 48 0.044
150
THY022 Thymic Carcinoma 48 0.044
151
PNC033 Pancreas Adenocarcinoma 47 0.044
152
c GGN002 Gigantism 47 0.044
153
FLL031 Follicular Adenoma 47 0.044
154
GRN017 Granulocytopenia 47 0.044
155
c ADL017 Adult T-Cell Leukemia 46 0.044
156
STC004 Stachybotrys Chartarum 46 0.044
157
LKP003 Leukoplakia 46 0.044
158
HMN016 Hemangioendothelioma 45 0.044
159
P OST051 Osteopetrosis Autosomal Recessive 1 45 0.044
160
ZYG002 Zygomycosis 44 0.044
161
c MSN006 Mesenchymoma 42 0.044
162
MTC010 Mitochondrial Dna Depletion Syndrome 42 0.044
163
ENC017 Encephaloceles 42 0.044
164
FBR002 Fibrosarcoma of Bone 41 0.044
165
c HMN021 Human T-Cell Leukemia Virus Type 1 41 0.044
166
P ATX010 Ataxia Neuropathy Spectrum 41 0.044
167
c CHR253 Chromosome 5q Deletion 39 0.044
168
VRL011 Viral Infectious Disease 36 0.044
169
CNG069 Congenital Cytomegalovirus 36 0.044
170
XLN003 X-Linked Sideroblastic Anemia with Ataxia 34 0.044
171
HMR001 Hemorrhagic Thrombocythemia 33 0.044
172
SYN053 Syndromic Diarrhea 32 0.044
173
c NTR033 Neutropenia, Severe Congenital 1, Autosomal Dominant 28 0.044
174
DFF022 Diffuse Neonatal Hemangiomatosis 25 0.044
175
c BNG012 Benign Mesenchymoma 22 0.044
176
c BNG076 Benign Exophthalmos Syndrome 22 0.044
177
MN1001 Mn1 21 0.044
178
AND005 Androgen Insensitivity Syndrome, Mild 21 0.044
179
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 17 0.044
180
PRS024 Parasagittal Meningioma 17 0.044
181
RDT014 Radiation Myelitis 15 0.044