Search results for hematopoiesis

185 hits were found for hematopoiesis

# Family MCID Name MIFTS Score
1
NTR040 Neutropenia, Cyclic 51 5.795
2
P LKM002 Leukemia 71 0.312
3
P MYL005 Myelofibrosis 67 0.212
4
P APL001 Aplastic Anemia 75 0.208
5
P THL005 Thalassemia 64 0.203
6
MYL009 Myelodysplastic Syndrome 73 0.179
7
P MYL006 Myeloid Leukemia 66 0.162
8
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.162
9
HMG002 Hemoglobinuria 48 0.162
10
P HRD011 Hereditary Spherocytosis 54 0.144
11
P PLY018 Polycythemia 58 0.106
12
END072 Endotheliitis 42 0.106
13
HMT018 Hematopoietic Stem Cell Transplantation 41 0.106
14
P OST001 Osteopetrosis 63 0.097
15
THL017 Thalassemia Intermedia 40 0.097
16
P BRS047 Breast Cancer 100 0.087
17
P LYM118 Lymphoma 69 0.087
18
c ACT073 Acute Leukemia 60 0.087
19
SPL018 Splenomegaly 44 0.087
20
MDS022 Mediastinitis 41 0.087
21
P NTR004 Neutropenia 59 0.075
22
P PNC001 Pancytopenia 52 0.075
23
BNM001 Bone Marrow Cancer 51 0.075
24
PRP016 Paraplegia 49 0.075
25
P TCL004 T-Cell Leukemia 47 0.075
26
c HMG003 Hemoglobin E Disease 44 0.075
27
PYG006 Pyogenic Granuloma 41 0.075
28
c PRM023 Pre-Malignant Neoplasm 41 0.075
29
P CNG003 Congenital Dyserythropoietic Anemia 40 0.075
30
MRG013 Mirage Syndrome 29 0.075
31
PRM243 Primary Bone Cancer 29 0.075
32
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 28 0.075
33
P MLT019 Multiple Myeloma 83 0.061
34
HV1006 Hiv-1 80 0.061
35
P ESS003 Essential Thrombocythemia 70 0.061
36
SVR004 Severe Combined Immunodeficiency 69 0.061
37
HMT002 Hematologic Cancer 64 0.061
38
c ADL017 Adult T-Cell Leukemia 60 0.061
39
MYL031 Myeloproliferative Neoplasm 58 0.061
40
PYR013 Pyruvate Kinase Deficiency 58 0.061
41
BNC003 Bone Cancer 58 0.061
42
CHR285 Chronic Myelomonocytic Leukemia 56 0.061
43
THR004 Thrombocytosis 55 0.061
44
HPT022 Hepatoblastoma 55 0.061
45
CYT008 Cytomegalovirus Infection 52 0.061
46
BNF002 Bone Fracture 50 0.061
47
CSY001 C Syndrome 50 0.061
48
THL018 Thalassemia Major 48 0.061
49
HMN009 Hemangioblastoma 45 0.061
50
RFR010 Refractory Anemia 45 0.061
51
PRN011 Pernicious Anemia 44 0.061
52
MCR017 Macrocytic Anemia 42 0.061
53
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.061
54
P SDR003 Sideroblastic Anemia 40 0.061
55
BNT003 Bent Bone Dysplasia Syndrome 37 0.061
56
MN1001 Mn1 30 0.061
57
c NTR033 Neutropenia, Severe Congenital 1, Autosomal Dominant 23 0.061
58
P OBS005 Obesity 92 0.043
59
P PRS040 Prostate Cancer 90 0.043
60
P RHM011 Rheumatoid Arthritis 89 0.043
61
P PLM037 Pulmonary Hypertension 79 0.043
62
P ART022 Arthritis 75 0.043
63
c LKM061 Leukemia, Acute Myeloid 73 0.043
64
P FLL037 Follicular Lymphoma 70 0.043
65
TBR010 Tuberculosis 70 0.043
66
P ADN016 Adenocarcinoma 69 0.043
67
P DMN001 Diamond-Blackfan Anemia 69 0.043
68
P HPT021 Hepatitis 69 0.043
69
P MNN013 Meningitis 67 0.043
70
P KDN018 Kidney Disease 66 0.043
71
DWN001 Down Syndrome 66 0.043
72
SRC014 Sarcoma 66 0.043
73
ATH003 Atherosclerosis 65 0.043
74
P AST007 Astrocytoma 65 0.043
75
CHD001 Chediak-Higashi Syndrome 64 0.043
76
P THR014 Thrombocytopenia 64 0.043
77
P OST002 Osteoporosis 64 0.043
78
P DYS007 Dyskeratosis Congenita 63 0.043
79
P HYP098 Hypereosinophilic Syndrome 63 0.043
80
P HLP001 Holoprosencephaly 63 0.043
81
PLY125 Polycythemia Vera, Somatic 63 0.043
82
PRT036 Peritonitis 63 0.043
83
P GCH001 Gaucher's Disease 62 0.043
84
P LYM026 Lymphoblastic Leukemia 62 0.043
85
P ASP006 Aspergillosis 61 0.043
86
P ESP024 Esophagitis 61 0.043
87
P PNC044 Pancreatitis 61 0.043
88
APP008 Appendicitis 60 0.043
89
WLL001 Williams-Beuren Syndrome 60 0.043
90
P PLC011 Pilocytic Astrocytoma 60 0.043
91
P HMN010 Hemangioma 59 0.043
92
OCL009 Ocular Cancer 59 0.043
93
DPH001 Diphtheria 59 0.043
94
P CTR002 Cataract 58 0.043
95
ADN018 Adenoma 58 0.043
96
TNG003 Tongue Cancer 58 0.043
97
P HST010 Histiocytosis 58 0.043
98
P EXN002 Exanthem 57 0.043
99
EXF001 Exfoliation Syndrome 57 0.043
100
P INT070 Intestinal Obstruction 57 0.043
101
c PRC016 Pre-Eclampsia 56 0.043
102
PLS011 Plasmacytoma 56 0.043
103
P FBR017 Fibrosarcoma 56 0.043
104
P TMT001 Timothy Syndrome 55 0.043
105
GRY002 Gray Platelet Syndrome 55 0.043
106
P RTH001 Rothmund-Thomson Syndrome 55 0.043
107
P MNC007 Monocytic Leukemia 55 0.043
108
P HYP345 Hyper-Ige Recurrent Infection Syndrome 54 0.043
109
P THY032 Thyroiditis 54 0.043
110
LYM022 Lymphangioma 54 0.043
111
P ECL001 Eclampsia 54 0.043
112
LST001 Listeriosis 53 0.043
113
PNM008 Pneumothorax 53 0.043
114
P ATX004 Ataxia 53 0.043
115
P CNT005 Central Nervous System Lymphoma 53 0.043
116
ADL002 Adult Syndrome 52 0.043
117
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.043
118
MYL001 Myelitis 51 0.043
119
SCK005 Sickle Cell Disease 51 0.043
120
NDL013 Nodular Regenerative Hyperplasia 50 0.043
121
EXT010 Extramedullary Plasmacytoma 49 0.043
122
MSS002 Mass Syndrome 48 0.043
123
NPH003 Nephrocalcinosis 48 0.043
124
P ENC008 Encephalocele 48 0.043
125
CHR005 Chorioamnionitis 48 0.043
126
c INV001 Invasive Aspergillosis 47 0.043
127
NTR003 Natural Killer Cell Leukemia 47 0.043
128
DWR001 Dwarfism 47 0.043
129
PRR002 Pure Red-Cell Aplasia 47 0.043
130
HMS001 Hemosiderosis 46 0.043
131
BLD053 Blood Platelet Disease 46 0.043
132
EPT020 Epithelioid Hemangioendothelioma 45 0.043
133
P PLN008 Peeling Skin Syndrome 45 0.043
134
VSC047 Vascular Malformation 45 0.043
135
c MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 44 0.043
136
CHR008 Choroiditis 44 0.043
137
CRD001 Cardiac Tamponade 44 0.043
138
HYD012 Hydrops Fetalis 43 0.043
139
LKC003 Leukocyte Disease 43 0.043
140
FLL031 Follicular Adenoma 42 0.043
141
c CHR064 Chronic Monocytic Leukemia 42 0.043
142
c NTR038 Neutropenia, Severe Congenital 3, Autosomal Recessive 41 0.043
143
HST016 Histiocytic Sarcoma 40 0.043
144
FBR002 Fibrosarcoma of Bone 40 0.043
145
c PLN018 Peeling Skin Syndrome 2 40 0.043
146
BND014 Bone Development Disease 40 0.043
147
TNG004 Tongue Disease 39 0.043
148
THL010 Thalassemia Minor 39 0.043
149
HMN016 Hemangioendothelioma 39 0.043
150
SPC003 Specific Developmental Disorder 38 0.043
151
ACT113 Acute Myeloblastic Leukemia with Maturation 37 0.043
152
BNS002 Bone Structure Disease 37 0.043
153
CNG069 Congenital Cytomegalovirus 36 0.043
154
SVR077 Severe Combined Immune Deficiency 36 0.043
155
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 36 0.043
156
c ACT020 Acute T Cell Leukemia 35 0.043
157
GRN039 Greenberg Skeletal Dysplasia 35 0.043
158
c PLN017 Peeling Skin Syndrome 1 34 0.043
159
c OST129 Osteopetrosis, Autosomal Recessive 2 34 0.043
160
c OST126 Osteopetrosis, Autosomal Recessive 1 34 0.043
161
ACR002 Acrocapitofemoral Dysplasia 33 0.043
162
P MSN006 Mesenchymoma 33 0.043
163
GGN002 Gigantism 32 0.043
164
LYM095 Lymphangiomatosis 32 0.043
165
XLN003 X-Linked Sideroblastic Anemia with Ataxia 32 0.043
166
OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 31 0.043
167
HNS001 Hansen's Disease 30 0.043
168
ACT118 Acute Non Lymphoblastic Leukemia 30 0.043
169
ACT114 Acute Myeloblastic Leukemia Without Maturation 29 0.043
170
NTR036 Neutropenia, Severe Congenital, X-Linked 28 0.043
171
c BNG012 Benign Mesenchymoma 28 0.043
172
OST097 Osteoporotic Fracture 28 0.043
173
c NTR039 Neutropenia, Severe Congenital 4, Autosomal Recessive 27 0.043
174
PRS024 Parasagittal Meningioma 26 0.043
175
BNM011 Bone Marrow Failure Syndrome 2 25 0.043
176
HMX002 Heme Oxygenase-1 Deficiency 25 0.043
177
DFF022 Diffuse Neonatal Hemangiomatosis 21 0.043
178
c PRX067 Paroxysmal Nocturnal Hemoglobinuria 2 21 0.043
179
c NTR034 Neutropenia, Severe Congenital, 6, Autosomal Recessive 20 0.043
180
c NTR037 Neutropenia, Severe Congenital 2, Autosomal Dominant 20 0.043
181
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 20 0.043
182
RDT014 Radiation Myelitis 18 0.043
183
WHT007 White Platelet Syndrome 15 0.043
184
CHK002 Cheek Mucosa Cancer 14 0.043
185
c NTR043 Neutropenia, Severe Congenital 7, Autosomal Recessive 12 0.043
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