Search results for hematopoiesis

210 hits were found for hematopoiesis

# Family MCID Name MIFTS Score
1
CYC010 Cyclic Neutropenia 52 5.842
2
P LKM002 Leukemia 75 0.318
3
P MYL005 Myelofibrosis 75 0.219
4
P THL005 Thalassemia 65 0.207
5
APL001 Aplastic Anemia 74 0.199
6
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.199
7
MYL009 Myelodysplastic Syndrome 75 0.176
8
P MYL006 Myeloid Leukemia 69 0.176
9
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.155
10
HMG002 Hemoglobinuria 52 0.155
11
c LKM061 Leukemia, Acute Myeloid 81 0.143
12
P HRD011 Hereditary Spherocytosis 55 0.143
13
c BTT014 Beta-Thalassemia 70 0.124
14
PLY001 Polycythemia Vera 75 0.117
15
P PLY018 Polycythemia 60 0.110
16
END072 Endotheliitis 46 0.110
17
c BLD140 Blood Group, I System 37 0.110
18
HMT018 Hematopoietic Stem Cell Transplantation 58 0.101
19
c LKM063 Leukemia, Chronic Myeloid 80 0.093
20
P LYM118 Lymphoma 71 0.093
21
P OST001 Osteopetrosis 70 0.093
22
P HRD009 Hereditary Wilms' Tumor 46 0.093
23
MDS022 Mediastinitis 44 0.093
24
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 29 0.093
25
P BRS047 Breast Cancer 100 0.083
26
SPL018 Splenomegaly 45 0.083
27
AGN016 Aging 65 0.072
28
MYL031 Myeloproliferative Neoplasm 64 0.072
29
P CHR285 Chronic Myelomonocytic Leukemia 63 0.072
30
c ACT073 Acute Leukemia 61 0.072
31
P NTR004 Neutropenia 60 0.072
32
PRP016 Paraplegia 53 0.072
33
PNC001 Pancytopenia 50 0.072
34
PYG006 Pyogenic Granuloma 45 0.072
35
P CNG003 Congenital Dyserythropoietic Anemia 42 0.072
36
BNT003 Bent Bone Dysplasia Syndrome 39 0.072
37
c HMG003 Hemoglobin E Disease 34 0.072
38
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 29 0.072
39
MYL069 Myeloma, Multiple 86 0.059
40
P PLM037 Pulmonary Hypertension 79 0.059
41
P HPT021 Hepatitis 75 0.059
42
P GRF003 Graft-Versus-Host Disease 72 0.059
43
SVR004 Severe Combined Immunodeficiency 71 0.059
44
P ADN016 Adenocarcinoma 71 0.059
45
P ESS003 Essential Thrombocythemia 71 0.059
46
c WLM013 Wilms Tumor 1 69 0.059
47
P DYS007 Dyskeratosis Congenita 68 0.059
48
P PNC044 Pancreatitis 64 0.059
49
CMB081 Combined Immunodeficiency, X-Linked 64 0.059
50
CYT008 Cytomegalovirus Infection 57 0.059
51
BNF002 Bone Fracture 56 0.059
52
HMN009 Hemangioblastoma 56 0.059
53
HPT022 Hepatoblastoma 55 0.059
54
THR004 Thrombocytosis 55 0.059
55
END081 Endosteal Hyperostosis, Autosomal Dominant 55 0.059
56
PYR041 Pyruvate Kinase Deficiency of Red Cells 54 0.059
57
PRN011 Pernicious Anemia 50 0.059
58
HMS001 Hemosiderosis 50 0.059
59
P TCL004 T-Cell Leukemia 50 0.059
60
c WLM018 Wilms Tumor 5 49 0.059
61
RFR010 Refractory Anemia 48 0.059
62
c WLM011 Wilms Tumor 6 44 0.059
63
MCR017 Macrocytic Anemia 44 0.059
64
P SDR003 Sideroblastic Anemia 43 0.059
65
c OST129 Osteopetrosis, Autosomal Recessive 2 33 0.059
66
c OST163 Osteopetrosis, Autosomal Recessive 3 33 0.059
67
MN1001 Mn1 32 0.059
68
c NTR047 Neutropenia, Severe Congenital, 1, Autosomal Dominant 32 0.059
69
P HMG026 Hemoglobin E-Beta-Thalassemia Syndrome 20 0.059
70
P RHM011 Rheumatoid Arthritis 91 0.041
71
P PRS040 Prostate Cancer 88 0.041
72
P ART022 Arthritis 77 0.041
73
P FLL037 Follicular Lymphoma 76 0.041
74
P OST002 Osteoporosis 75 0.041
75
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.041
76
c CHR089 Chronic Kidney Failure 72 0.041
77
VSC007 Vascular Disease 71 0.041
78
P MNN013 Meningitis 71 0.041
79
BRK010 Burkitt Lymphoma 71 0.041
80
DWN001 Down Syndrome 70 0.041
81
P DMN001 Diamond-Blackfan Anemia 70 0.041
82
c MNN043 Meningioma, Familial 69 0.041
83
P KDN018 Kidney Disease 69 0.041
84
P AMY004 Amyloidosis 69 0.041
85
P MYC084 Mycobacterium Tuberculosis 1 69 0.041
86
SRC014 Sarcoma 68 0.041
87
PNC041 Pancreatic Ductal Adenocarcinoma 67 0.041
88
P HLP001 Holoprosencephaly 67 0.041
89
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.041
90
CHD001 Chediak-Higashi Syndrome 67 0.041
91
PRT036 Peritonitis 67 0.041
92
P AST007 Astrocytoma 66 0.041
93
P LYM026 Lymphoblastic Leukemia 66 0.041
94
P ASP006 Aspergillosis 65 0.041
95
c PRC016 Pre-Eclampsia 65 0.041
96
P HYP098 Hypereosinophilic Syndrome 65 0.041
97
P THR014 Thrombocytopenia 65 0.041
98
MCC012 Mccune-Albright Syndrome 65 0.041
99
APP008 Appendicitis 64 0.041
100
P ESP024 Esophagitis 64 0.041
101
HMT002 Hematologic Cancer 64 0.041
102
ADN018 Adenoma 63 0.041
103
LNG108 Langerhans Cell Histiocytosis 63 0.041
104
PNC033 Pancreas Adenocarcinoma 63 0.041
105
DPH001 Diphtheria 63 0.041
106
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.041
107
c ADL017 Adult T-Cell Leukemia 63 0.041
108
PRP001 Propionic Acidemia 63 0.041
109
P PLC011 Pilocytic Astrocytoma 63 0.041
110
P ART021 Arteriosclerosis 62 0.041
111
P GCH001 Gaucher's Disease 62 0.041
112
P EXN002 Exanthem 62 0.041
113
P HMN010 Hemangioma 61 0.041
114
P FBR017 Fibrosarcoma 61 0.041
115
P CTR002 Cataract 60 0.041
116
MNT002 Mental Depression 60 0.041
117
c ALP101 Alpha-Thalassemia 60 0.041
118
P NPH012 Nephrotic Syndrome 60 0.041
119
P HST010 Histiocytosis 60 0.041
120
PLS011 Plasmacytoma 60 0.041
121
PST028 Post-Traumatic Stress Disorder 59 0.041
122
P MNC007 Monocytic Leukemia 59 0.041
123
P CRN038 Carney Complex Variant 59 0.041
124
PRT118 Protoporphyria, Erythropoietic 58 0.041
125
P ECL001 Eclampsia 57 0.041
126
P RTH001 Rothmund-Thomson Syndrome 57 0.041
127
P CNT005 Central Nervous System Lymphoma 57 0.041
128
PNM008 Pneumothorax 57 0.041
129
c ALM001 Al Amyloidosis 56 0.041
130
P THY032 Thyroiditis 56 0.041
131
GRY002 Gray Platelet Syndrome 56 0.041
132
P INT070 Intestinal Obstruction 55 0.041
133
P MMB011 Membranous Nephropathy 55 0.041
134
c ANM036 Anemia, Sideroblastic, 1 55 0.041
135
LST001 Listeriosis 55 0.041
136
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 54 0.041
137
SCK005 Sickle Cell Disease 54 0.041
138
LYM022 Lymphangioma 53 0.041
139
NDL013 Nodular Regenerative Hyperplasia 53 0.041
140
P HMN036 Hemangiopericytoma, Malignant 52 0.041
141
EXT010 Extramedullary Plasmacytoma 52 0.041
142
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.041
143
CHR005 Chorioamnionitis 52 0.041
144
MYL001 Myelitis 52 0.041
145
PRR002 Pure Red-Cell Aplasia 52 0.041
146
c AMG001 Amegakaryocytic Thrombocytopenia, Congenital 51 0.041
147
c INV001 Invasive Aspergillosis 51 0.041
148
HYD012 Hydrops Fetalis 50 0.041
149
P EPT020 Epithelioid Hemangioendothelioma 50 0.041
150
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.041
151
TTR011 Tetraploidy 49 0.041
152
NPH003 Nephrocalcinosis 49 0.041
153
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.041
154
P ENC008 Encephalocele 48 0.041
155
DWR001 Dwarfism 48 0.041
156
LKC005 Leukocyte Adhesion Deficiency, Type Iii 47 0.041
157
CHR008 Choroiditis 47 0.041
158
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.041
159
c MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 47 0.041
160
ESP002 Esophageal Varix 46 0.041
161
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.041
162
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.041
163
NTR003 Natural Killer Cell Leukemia 45 0.041
164
HST016 Histiocytic Sarcoma 45 0.041
165
BLD053 Blood Platelet Disease 45 0.041
166
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.041
167
CRD001 Cardiac Tamponade 45 0.041
168
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.041
169
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 43 0.041
170
RTR011 Retroperitoneal Fibrosis 43 0.041
171
HMN016 Hemangioendothelioma 43 0.041
172
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.041
173
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.041
174
PNM010 Pneumothorax, Primary Spontaneous 41 0.041
175
OST097 Osteoporotic Fracture 41 0.041
176
FLL031 Follicular Adenoma 41 0.041
177
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.041
178
CNG069 Congenital Cytomegalovirus 40 0.041
179
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.041
180
IMM078 Immunodeficiency 21 38 0.041
181
c CTR122 Cataract 5, Multiple Types 38 0.041
182
P MSN006 Mesenchymoma 37 0.041
183
PPL059 Popliteal Pterygium Syndrome, Lethal Type 37 0.041
184
c OST126 Osteopetrosis, Autosomal Recessive 1 36 0.041
185
c NTR049 Neutropenia, Severe Congenital, 3, Autosomal Recessive 36 0.041
186
GRN013 Greenberg Dysplasia 36 0.041
187
FBR002 Fibrosarcoma of Bone 36 0.041
188
GGN002 Gigantism 36 0.041
189
LYM095 Lymphangiomatosis 35 0.041
190
EMP011 Emphysema, Congenital Lobar 35 0.041
191
HYD059 Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect 34 0.041
192
ACT118 Acute Non Lymphoblastic Leukemia 32 0.041
193
c NTR050 Neutropenia, Severe Congenital, 4, Autosomal Recessive 32 0.041
194
P RNG031 Ring Chromosome Y Syndrome 29 0.041
195
P STR035 Streptococcal Group a Invasive Disease 28 0.041
196
HMX003 Heme Oxygenase 1 Deficiency 26 0.041
197
DFF022 Diffuse Neonatal Hemangiomatosis 26 0.041
198
CLC064 Calcifying Aponeurotic Fibroma 26 0.041
199
PRS024 Parasagittal Meningioma 25 0.041
200
INF158 Infections, Recurrent, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations 24 0.041
201
c BNG012 Benign Mesenchymoma 24 0.041
202
NTR036 Neutropenia, Severe Congenital, X-Linked 23 0.041
203
c NTR034 Neutropenia, Severe Congenital, 6, Autosomal Recessive 21 0.041
204
c FTL067 Fetal Hemoglobin Quantitative Trait Locus 6 21 0.041
205
c NTR051 Neutropenia, Severe Congenital, 2, Autosomal Dominant 21 0.041
206
BNM011 Bone Marrow Failure Syndrome 2 20 0.041
207
c NTR044 Neutropenia, Severe Congenital, 7, Autosomal Recessive 20 0.041
208
c PRX094 Paroxysmal Nocturnal Hemoglobinuria 1 19 0.041
209
c PRX067 Paroxysmal Nocturnal Hemoglobinuria 2 17 0.041
210
RDT014 Radiation Myelitis 17 0.041
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