Search results for dyserythropoietic anemia

114 hits were found for dyserythropoietic anemia

# Family MCID Name MIFTS Score
1
c ANM043 Anemia, Congenital Dyserythropoietic, Type Ia 37 9.405
2
c ANM042 Anemia, Congenital Dyserythropoietic, Type Ii 32 9.261
3
P CNG003 Congenital Dyserythropoietic Anemia 42 8.887
4
c ANM037 Anemia, Congenital Dyserythropoietic, Type Iii 31 7.439
5
c ANM048 Anemia, Congenital Dyserythropoietic, Type Iv 26 7.195
6
THR097 Thrombocytopenia, X-Linked, with or Without Dyserythropoietic Anemia 22 5.998
7
c ANM049 Anemia, Congenital Dyserythropoietic, Type Ib 23 5.567
8
MJD001 Majeed Syndrome 35 5.552
9
EXC004 Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis 22 5.219
10
DYS127 Dyserythropoietic Anemia and Thrombocytopenia 20 4.114
11
BTT013 Beta-Thalassemia, Dominant Inclusion Body Type 22 3.177
12
c BLD140 Blood Group, I System 37 0.509
13
P HML002 Hemolytic Anemia 62 0.439
14
IRN002 Iron Metabolism Disease 45 0.342
15
DFC004 Deficiency Anemia 62 0.340
16
IRN001 Iron Deficiency Anemia 55 0.334
17
PRN011 Pernicious Anemia 50 0.278
18
P LKM002 Leukemia 75 0.262
19
P THL005 Thalassemia 65 0.254
20
P MGL001 Megaloblastic Anemia 52 0.251
21
P SDR003 Sideroblastic Anemia 43 0.214
22
HMS001 Hemosiderosis 50 0.213
23
MCR017 Macrocytic Anemia 44 0.200
24
MYL009 Myelodysplastic Syndrome 75 0.195
25
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.189
26
c BTT014 Beta-Thalassemia 70 0.188
27
P THR014 Thrombocytopenia 65 0.187
28
P ANR048 Aniridia 1 68 0.185
29
ANR038 Anorexia Nervosa 1 21 0.185
30
BLD137 Blood Group--Ahonen 17 0.185
31
HMT018 Hematopoietic Stem Cell Transplantation 58 0.180
32
AGN016 Aging 65 0.166
33
c CNG027 Congenital Hemolytic Anemia 46 0.160
34
MCR018 Microcytic Anemia 43 0.159
35
ALR002 Al-Raqad Syndrome 30 0.158
36
P HRD011 Hereditary Spherocytosis 55 0.156
37
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.151
38
HYD012 Hydrops Fetalis 50 0.142
39
SPL018 Splenomegaly 45 0.142
40
HYD059 Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect 34 0.141
41
CRB009 Cerebritis 41 0.134
42
PYR041 Pyruvate Kinase Deficiency of Red Cells 54 0.127
43
HPT082 Hepatic Adenomas, Familial 52 0.127
44
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 41 0.126
45
CRN237 Corneal Dystrophy, Avellino Type 36 0.119
46
MYL069 Myeloma, Multiple 86 0.118
47
CNG034 Congestive Heart Failure 74 0.118
48
OST017 Osteomyelitis 64 0.116
49
P LVR013 Liver Disease 76 0.116
50
P PLM037 Pulmonary Hypertension 79 0.114
51
P DYS007 Dyskeratosis Congenita 68 0.113
52
THR024 Thrombosis 61 0.109
53
CHR288 Chronic Recurrent Multifocal Osteomyelitis 55 0.109
54
HRY003 Hairy Cell Leukemia 60 0.108
55
VTM002 Vitamin B12 Deficiency 46 0.106
56
P ANT006 Antiphospholipid Syndrome 59 0.106
57
ALP046 Alport Syndrome, X-Linked 74 0.105
58
PRP030 Purpura 61 0.103
59
RTN023 Retinitis 52 0.101
60
ANG004 Angioid Streaks 35 0.097
61
ACT098 Acute Erythroid Leukemia 52 0.095
62
MDS022 Mediastinitis 44 0.095
63
c HMC039 Hemochromatosis, Type 1 71 0.092
64
PRP007 Priapism 49 0.092
65
GRN017 Granulocytopenia 49 0.092
66
ADP007 Adie Pupil 41 0.089
67
P PNC044 Pancreatitis 64 0.087
68
IMM158 Immune Suppression 57 0.087
69
GLC009 Glucosephosphate Dehydrogenase Deficiency 48 0.083
70
P HPT023 Hepatocellular Carcinoma 94 0.081
71
GT001 Gout 60 0.080
72
P PLM006 Pulmonary Alveolar Proteinosis 49 0.080
73
P ATR010 Atrial Heart Septal Defect 45 0.076
74
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.076
75
c ELL005 Elliptocytosis 2 29 0.076
76
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 20 0.074
77
c THR071 Thrombocytopenia 1 48 0.074
78
UND005 Undifferentiated Pleomorphic Sarcoma 59 0.072
79
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.070
80
GLB001 Gilbert Syndrome 55 0.069
81
HDC001 Headache 55 0.069
82
ECT006 Ectodermal Dysplasia 57 0.069
83
P SCL018 Scoliosis 56 0.069
84
DBN001 Dubin-Johnson Syndrome 56 0.069
85
ACR013 Acrodysostosis 53 0.069
86
FBR032 Fibromuscular Dysplasia 53 0.069
87
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 24 0.069
88
P RNL007 Renal Tubular Acidosis 51 0.067
89
PST092 Posttransplant Acute Limbic Encephalitis 11 0.067
90
RPP001 Rapp-Hodgkin Syndrome 51 0.066
91
P RNL045 Renal Tubular Acidosis, Distal 42 0.066
92
c CNG208 Congenital Disorder of Glycosylation, Type Iic 42 0.066
93
TTR025 Tetraamelia Syndrome, Autosomal Recessive 40 0.066
94
c TRC078 Trichohepatoenteric Syndrome 2 34 0.066
95
HYP068 Hyperostosis 52 0.064
96
c ALZ056 Alzheimer Disease 3 41 0.064
97
P ANX007 Anauxetic Dysplasia 1 36 0.064
98
CMB083 Combined Immunodeficiency and Megaloblastic Anemia with or Without Hyperhomocysteinemia 15 0.064
99
c HMC010 Hemochromatosis, Type 3 42 0.060
100
OVL001 Ovalocytosis, Southeast Asian 30 0.060
101
NNT012 Neonatal Jaundice 51 0.058
102
ERY051 Erythroleukemia, Familial 26 0.058
103
BNF002 Bone Fracture 56 0.055
104
NTR042 Neutrophilic Dermatosis, Acute Febrile 31 0.055
105
c EPL183 Epileptic Encephalopathy, Early Infantile, 50 25 0.055
106
EXC002 Exocrine Pancreatic Insufficiency 45 0.053
107
CLV004 Calvarial Hyperostosis 29 0.053
108
P JVN024 Juvenile Hereditary Hemochromatosis 22 0.053
109
DYS197 Dyserythropoiesis, Congenital, with Ultrastructurally Normal Erythroblast Heterochromatin 11 0.053
110
ICH002 Ichthyosis Bullosa of Siemens 48 0.049
111
P FNG006 Feingold Syndrome 1 44 0.049
112
c PRM225 Primary Thrombocytopenia 37 0.049
113
MDS018 Mediastinal Cancer 35 0.049
114
GT1001 Gata1-Related X-Linked Cytopenia 2 0.049
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