Search results for dyserythropoietic anemia

202 hits were found for dyserythropoietic anemia

# Family MCID Name MIFTS Score
1
c DYS170 Dyserythropoietic Anemia, Congenital, Type Ii 28 8.723
2
c DYS156 Dyserythropoietic Anemia, Congenital, Type Ia 35 8.614
3
P CNG003 Congenital Dyserythropoietic Anemia 40 7.669
4
c DYS168 Dyserythropoietic Anemia, Congenital, Type Iv 25 7.132
5
c DYS167 Dyserythropoietic Anemia, Congenital, Type Iii 23 6.808
6
c DYS155 Dyserythropoietic Anemia, Congenital, Type Ib 23 5.685
7
THR097 Thrombocytopenia, X-Linked, with or Without Dyserythropoietic Anemia 18 5.268
8
EXC004 Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis 21 4.936
9
MJD001 Majeed Syndrome 33 4.815
10
DYS127 Dyserythropoietic Anemia and Thrombocytopenia 17 3.890
11
THR108 Thrombocytopenia with or Without Dyserythropoietic Anemia 12 3.748
12
GT1003 Gata1-Related Anemia with Thrombocytopenia 3 2.404
13
GT1004 Gata1-Related Cytopenia 5 2.155
14
THL011 Thalassemia-Beta, Dominant Inclusion-Body 21 2.142
15
P HML002 Hemolytic Anemia 62 0.414
16
DFC004 Deficiency Anemia 64 0.395
17
IRN001 Iron Deficiency Anemia 52 0.295
18
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.272
19
P LKM002 Leukemia 71 0.210
20
P THL005 Thalassemia 64 0.206
21
P SDR003 Sideroblastic Anemia 40 0.190
22
c CNG027 Congenital Hemolytic Anemia 48 0.183
23
P THR014 Thrombocytopenia 64 0.169
24
MCR017 Macrocytic Anemia 42 0.165
25
HMT018 Hematopoietic Stem Cell Transplantation 41 0.161
26
P HMC003 Hemochromatosis 72 0.156
27
MRG013 Mirage Syndrome 29 0.152
28
NTR005 Nutritional Deficiency Disease 36 0.133
29
ALR002 Al-Raqad Syndrome 36 0.132
30
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.125
31
PYR013 Pyruvate Kinase Deficiency 58 0.123
32
SPL018 Splenomegaly 44 0.121
33
HMS001 Hemosiderosis 46 0.119
34
HYD012 Hydrops Fetalis 43 0.118
35
END030 End Stage Renal Failure 55 0.117
36
CRB009 Cerebritis 39 0.114
37
HPT074 Hepatic Adenoma, Somatic 50 0.109
38
P HRD011 Hereditary Spherocytosis 54 0.107
39
HNM002 Hinman Syndrome 25 0.106
40
CNG034 Congestive Heart Failure 72 0.101
41
CRN237 Corneal Dystrophy, Avellino Type 30 0.100
42
P LVR013 Liver Disease 75 0.100
43
P PLM037 Pulmonary Hypertension 79 0.099
44
P DYS007 Dyskeratosis Congenita 63 0.098
45
OST017 Osteomyelitis 61 0.097
46
THR024 Thrombosis 57 0.095
47
VTM002 Vitamin B12 Deficiency 44 0.093
48
HRY003 Hairy Cell Leukemia 57 0.093
49
CHR288 Chronic Recurrent Multifocal Osteomyelitis 45 0.092
50
AND005 Androgen Insensitivity Syndrome, Mild 16 0.091
51
PRP030 Purpura 58 0.088
52
CRR007 Cirrhosis, Cryptogenic 43 0.085
53
INC022 Inclusion-Cell Disease 46 0.083
54
c CRN214 Coronary Heart Disease 5 22 0.081
55
PRP007 Priapism 46 0.079
56
MDS022 Mediastinitis 41 0.079
57
P ANT006 Antiphospholipid Syndrome 56 0.078
58
GRN017 Granulocytopenia 44 0.078
59
P CRN178 Coronary Heart Disease 6 21 0.078
60
ADP007 Adie Pupil 34 0.076
61
THR042 Thrombocytopenia, X-Linked 45 0.075
62
PRT036 Peritonitis 63 0.074
63
c VRL010 Viral Hepatitis 60 0.074
64
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.073
65
RTN023 Retinitis 50 0.073
66
P PNC044 Pancreatitis 61 0.072
67
BND014 Bone Development Disease 40 0.071
68
ACR002 Acrocapitofemoral Dysplasia 33 0.071
69
IMM136 Immune System Disease 51 0.068
70
P GT001 Gout 58 0.067
71
KRT002 Keratomalacia 52 0.067
72
ACT098 Acute Erythroid Leukemia 47 0.067
73
c RNL016 Renal Infectious Disease 20 0.067
74
c HPT003 Hepatitis a 59 0.066
75
P END033 Endocarditis 54 0.066
76
P PLM006 Pulmonary Alveolar Proteinosis 48 0.065
77
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 33 0.065
78
P CHL066 Cholangitis 42 0.065
79
PYR009 Pyridoxine Deficiency Anemia 18 0.065
80
ACQ007 Acquired Immunodeficiency Syndrome 60 0.063
81
GST050 Gastrointestinal System Disease 56 0.063
82
KWS002 Kawasaki Disease 70 0.062
83
GST045 Gastroenteritis 59 0.062
84
ANM026 Anemia, X-Linked, with/without Neutropenia and/or Platelet Abnormalities 22 0.062
85
P RSP003 Respiratory Failure 71 0.060
86
P MNN013 Meningitis 67 0.060
87
PRT038 Protein-Energy Malnutrition 49 0.060
88
P SCL009 Sclerosing Cholangitis 48 0.060
89
CHL004 Cholelithiasis 48 0.060
90
P ATX010 Ataxia Neuropathy Spectrum 30 0.060
91
c CRN177 Coronary Heart Disease 7 20 0.060
92
c HPT016 Hepatitis B 64 0.058
93
HDC001 Headache 54 0.058
94
BRN106 Burns 52 0.058
95
TRY001 Trypanosomiasis 51 0.058
96
RNL007 Renal Tubular Acidosis 50 0.058
97
c PRM225 Primary Thrombocytopenia 39 0.058
98
TTR016 Tetra-Amelia Syndrome 36 0.058
99
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.058
100
PBL001 Piebaldism 57 0.058
101
P SCL018 Scoliosis 55 0.058
102
DBN001 Dubin-Johnson Syndrome 54 0.058
103
ECT006 Ectodermal Dysplasia 52 0.058
104
ACR013 Acrodysostosis 50 0.058
105
FBR032 Fibromuscular Dysplasia 43 0.058
106
GT1001 Gata1-Related X-Linked Cytopenia 3 0.058
107
SCH014 Schistosomiasis 58 0.057
108
c HPT007 Hepatitis E 54 0.057
109
P PYL005 Pyelonephritis 52 0.057
110
NRM003 Norum Disease 51 0.057
111
BCL002 B Cell Deficiency 49 0.057
112
RPP001 Rapp-Hodgkin Syndrome 48 0.057
113
P GLL020 Gallbladder Disease 59 0.055
114
ATS010 Autosomal Recessive Disease 41 0.055
115
c TRC078 Trichohepatoenteric Syndrome 2 29 0.055
116
APP008 Appendicitis 60 0.054
117
ALC006 Alcoholic Hepatitis 59 0.054
118
RSP006 Respiratory System Disease 58 0.054
119
CRT016 Carotid Artery Disease 57 0.054
120
VSC003 Visceral Leishmaniasis 56 0.054
121
P TRC086 Trichohepatoenteric Syndrome 1 48 0.054
122
HYP068 Hyperostosis 40 0.054
123
P PRT013 Portal Hypertension 60 0.052
124
P INT001 Intrahepatic Cholestasis 59 0.052
125
NDL013 Nodular Regenerative Hyperplasia 50 0.052
126
c EHL032 Ehlers-Danlos Syndrome, Type Viib 49 0.052
127
c HYP072 Hypersensitivity Reaction Type Iii Disease 38 0.052
128
ATS009 Autosomal Genetic Disease 35 0.052
129
HYD057 Hydrops Fetalis, Non-Immune, and/or Atrial Septal Defect 17 0.052
130
TNG002 Tangier Disease 62 0.050
131
HYP121 Hypoalphalipoproteinemia 61 0.050
132
FLR002 Filariasis 54 0.050
133
P ACQ009 Acquired Metabolic Disease 38 0.050
134
OTT002 Otitis Media 66 0.047
135
DNG002 Dengue Hemorrhagic Fever 63 0.047
136
P HYP117 Hypertriglyceridemia 61 0.047
137
TYP007 Typhoid Fever 61 0.047
138
LPD008 Lipid Metabolism Disorder 58 0.047
139
HMR004 Hemorrhagic Fever with Renal Syndrome 58 0.047
140
P HMR012 Hemorrhagic Fever 56 0.047
141
HPT019 Hepatic Encephalopathy 56 0.047
142
PLR022 Pleural Disease 51 0.047
143
HYP081 Hypolipoproteinemia 42 0.047
144
SVN001 Sveinsson Choreoretinal Atrophy 26 0.047
145
P HYP607 Hypercholesterolemia, Familial 76 0.045
146
P ALG002 Alagille Syndrome 72 0.045
147
BRN024 Bronchitis 64 0.045
148
LPP001 Lipoprotein Lipase Deficiency 63 0.045
149
ABT001 Abetalipoproteinemia 60 0.045
150
KRT001 Keratoconjunctivitis Sicca 59 0.045
151
c BCT007 Bacterial Meningitis 54 0.045
152
P HYP027 Hypobetalipoproteinemia 53 0.045
153
P HYP614 Hyperlipidemia, Familial Combined 50 0.045
154
BNF002 Bone Fracture 50 0.045
155
P HYP090 Hyperalphalipoproteinemia 48 0.045
156
P FML035 Familial Hyperlipidemia 48 0.045
157
OBS001 Obstructive Jaundice 48 0.045
158
P CMP008 Compartment Syndrome 48 0.045
159
LPP002 Lipoprotein Glomerulopathy 46 0.045
160
EXC002 Exocrine Pancreatic Insufficiency 43 0.045
161
CRB008 Cerebral Atherosclerosis 43 0.045
162
c HYP011 Hyperlipoproteinemia Type Iii 42 0.045
163
c LKD015 Leukodystrophy, Hypomyelinating, 3 42 0.045
164
c AMY009 Amyloidosis Aa 39 0.045
165
ARC001 Arcus Senilis 35 0.045
166
FML330 Familial Lcat Deficiency 34 0.045
167
DFC001 Defective Apolipoprotein B-100 29 0.045
168
c JVN024 Juvenile Hereditary Hemochromatosis 29 0.045
169
CLV004 Calvarial Hyperostosis 28 0.045
170
TNP002 Tinea Profunda 20 0.045
171
TTR001 Tetralogy of Fallot 71 0.041
172
HJD001 Hajdu-Cheney Syndrome 59 0.041
173
GLL022 Guillain-Barre Syndrome 56 0.041
174
P CDS001 Cadasil 55 0.041
175
NNT012 Neonatal Jaundice 50 0.041
176
HPT025 Hepatic Lipase Deficiency 48 0.041
177
HPT009 Hepatopulmonary Syndrome 48 0.041
178
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 46 0.041
179
c CHL120 Cholestasis, Benign Recurrent Intrahepatic 46 0.041
180
c CHL082 Cholestasis, Progressive Familial Intrahepatic 3 45 0.041
181
ICH002 Ichthyosis Bullosa of Siemens 45 0.041
182
P ATR010 Atrial Heart Septal Defect 45 0.041
183
HYP286 Hyperchylomicronemia, Late-Onset 45 0.041
184
c CHL081 Cholestasis, Progressive Familial Intrahepatic 2 45 0.041
185
FSH001 Fish-Eye Disease 43 0.041
186
TBR008 Tuberculous Peritonitis 41 0.041
187
GRN006 Granulomatous Angiitis 40 0.041
188
c HMC009 Hemochromatosis Type 2 39 0.041
189
c HMC010 Hemochromatosis, Type 3 39 0.041
190
TRC021 Tricuspid Valve Stenosis 39 0.041
191
c HMC035 Hemochromatosis, Type 4 39 0.041
192
c SPN297 Spondylocostal Dysostosis 3, Autosomal Recessive 37 0.041
193
SBL008 Sea-Blue Histiocyte Disease 36 0.041
194
MDS018 Mediastinal Cancer 36 0.041
195
CHR355 Chromosome 15q13.3 Microdeletion Syndrome 31 0.041
196
c HMC034 Hemochromatosis, Type 5 30 0.041
197
LWG002 Low Gamma-Gt Familial Intrahepatic Cholestasis 24 0.041
198
APD001 Apo a-I Deficiency 20 0.041
199
ARR033 Arrhythmogenic Right Ventricular Dysplasia 4 17 0.041
200
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 13 0.041
201
P TCL017 T-Cell Acute Lymphocytic Leukemia-1 10 0.041
202
P PBL002 Piebald Trait, Kit-Related 8 0.041
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