Search results for "dyserythropoietic anemia"

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

179 hits were found for 'dyserythropoietic anemia'

# Family MCID Name MIFTS Score
1
c DYS170 Dyserythropoietic Anemia, Congenital, Type Ii 29 8.663
2
c DYS156 Dyserythropoietic Anemia, Congenital, Type Ia 35 8.552
3
P CNG003 Congenital Dyserythropoietic Anemia 39 7.309
4
c DYS168 Dyserythropoietic Anemia, Congenital, Type Iv 25 7.080
5
c DYS167 Dyserythropoietic Anemia, Congenital, Type Iii 23 6.759
6
c DYS155 Dyserythropoietic Anemia, Congenital, Type Ib 23 5.643
7
THR097 Thrombocytopenia, X-Linked, with or Without Dyserythropoietic Anemia 19 5.230
8
EXC004 Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis 21 4.902
9
MJD001 Majeed Syndrome 33 4.778
10
DYS127 Dyserythropoietic Anemia and Thrombocytopenia 17 3.868
11
THR108 Thrombocytopenia with or Without Dyserythropoietic Anemia 12 3.722
12
GT1003 Gata1-Related Anemia with Thrombocytopenia 3 2.389
13
CRN237 Corneal Dystrophy, Avellino Type 30 2.246
14
GT1004 Gata1-Related Cytopenia 5 2.139
15
THL011 Thalassemia-Beta, Dominant Inclusion-Body 21 2.125
16
P HML002 Hemolytic Anemia 60 0.411
17
DFC004 Deficiency Anemia 65 0.389
18
IRN001 Iron Deficiency Anemia 51 0.291
19
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.268
20
P LKM002 Leukemia 70 0.219
21
P THL005 Thalassemia 61 0.207
22
P SDR003 Sideroblastic Anemia 39 0.188
23
c CNG027 Congenital Hemolytic Anemia 48 0.184
24
MYL009 Myelodysplastic Syndrome 74 0.172
25
P THR014 Thrombocytopenia 64 0.169
26
MCR017 Macrocytic Anemia 41 0.165
27
HMT018 Hematopoietic Stem Cell Transplantation 41 0.162
28
P HMC003 Hemochromatosis 72 0.159
29
MRG013 Mirage Syndrome 26 0.152
30
HMT002 Hematologic Cancer 64 0.134
31
NTR005 Nutritional Deficiency Disease 39 0.132
32
ALR002 Al-Raqad Syndrome 36 0.132
33
PYR013 Pyruvate Kinase Deficiency 58 0.124
34
SPL018 Splenomegaly 44 0.121
35
HYD012 Hydrops Fetalis 44 0.119
36
CRB009 Cerebritis 38 0.115
37
c ACT073 Acute Leukemia 62 0.109
38
P HRD011 Hereditary Spherocytosis 53 0.106
39
OST017 Osteomyelitis 59 0.102
40
CNG034 Congestive Heart Failure 71 0.102
41
P PLM037 Pulmonary Hypertension 79 0.100
42
P DYS007 Dyskeratosis Congenita 63 0.099
43
HPT074 Hepatic Adenoma, Somatic 51 0.096
44
HRY003 Hairy Cell Leukemia 60 0.095
45
CHR288 Chronic Recurrent Multifocal Osteomyelitis 45 0.094
46
VTM002 Vitamin B12 Deficiency 44 0.091
47
IMM127 Immune System Cancer 42 0.089
48
P LVR013 Liver Disease 72 0.088
49
PRP030 Purpura 59 0.088
50
CRR007 Cirrhosis, Cryptogenic 44 0.085
51
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.084
52
c LKM061 Leukemia, Acute Myeloid 71 0.083
53
MDS022 Mediastinitis 41 0.081
54
PRP007 Priapism 47 0.081
55
HNM002 Hinman Syndrome 25 0.081
56
c CRN214 Coronary Heart Disease 5 23 0.080
57
P ANT006 Antiphospholipid Syndrome 58 0.079
58
GRN017 Granulocytopenia 42 0.079
59
THR042 Thrombocytopenia, X-Linked 46 0.077
60
P CRN178 Coronary Heart Disease 6 24 0.077
61
UND005 Undifferentiated Pleomorphic Sarcoma 43 0.075
62
AND005 Androgen Insensitivity Syndrome, Mild 16 0.074
63
P PNC044 Pancreatitis 60 0.073
64
BND014 Bone Development Disease 42 0.073
65
RTN023 Retinitis 49 0.072
66
ACR002 Acrocapitofemoral Dysplasia 36 0.072
67
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.071
68
P GT001 Gout 58 0.070
69
ACT098 Acute Erythroid Leukemia 48 0.069
70
P PLM006 Pulmonary Alveolar Proteinosis 48 0.068
71
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 30 0.067
72
KRT002 Keratomalacia 54 0.067
73
c RNL016 Renal Infectious Disease 24 0.067
74
PYR009 Pyridoxine Deficiency Anemia 21 0.064
75
ANM026 Anemia, X-Linked, with/without Neutropenia and/or Platelet Abnormalities 24 0.063
76
c PRM225 Primary Thrombocytopenia 42 0.061
77
PBL001 Piebaldism 57 0.060
78
P SCL018 Scoliosis 56 0.060
79
DBN001 Dubin-Johnson Syndrome 52 0.060
80
ACR013 Acrodysostosis 49 0.060
81
ECT006 Ectodermal Dysplasia 47 0.060
82
FBR032 Fibromuscular Dysplasia 45 0.060
83
GT1001 Gata1-Related X-Linked Cytopenia 3 0.060
84
HDC001 Headache 54 0.059
85
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.059
86
CHL068 Cholestasis 58 0.058
87
RNL007 Renal Tubular Acidosis 50 0.058
88
BCL002 B Cell Deficiency 50 0.058
89
RPP001 Rapp-Hodgkin Syndrome 48 0.058
90
CHR563 Chronic Eosinophilic Leukemia 47 0.058
91
c CRN177 Coronary Heart Disease 7 22 0.058
92
NRM003 Norum Disease 52 0.056
93
ATS010 Autosomal Recessive Disease 41 0.056
94
c TRC078 Trichohepatoenteric Syndrome 2 31 0.056
95
HYP068 Hyperostosis 40 0.054
96
P ATX010 Ataxia Neuropathy Spectrum 28 0.054
97
NDL013 Nodular Regenerative Hyperplasia 49 0.053
98
ATS009 Autosomal Genetic Disease 39 0.053
99
P INT001 Intrahepatic Cholestasis 57 0.051
100
LKM067 Leukemia, Acute Promyelocytic, Somatic 53 0.051
101
MYL003 Myeloid Sarcoma 48 0.051
102
ACT113 Acute Myeloblastic Leukemia with Maturation 40 0.051
103
ACT114 Acute Myeloblastic Leukemia Without Maturation 30 0.051
104
c JVN024 Juvenile Hereditary Hemochromatosis 28 0.051
105
HYP121 Hypoalphalipoproteinemia 61 0.048
106
P GLM045 Glioma 58 0.048
107
BNF002 Bone Fracture 47 0.048
108
ENC044 Enchondromatosis, Multiple, Ollier Type 44 0.048
109
CRB138 Core Binding Factor Acute Myeloid Leukemia 41 0.048
110
c HMC010 Hemochromatosis, Type 3 38 0.048
111
c HMC009 Hemochromatosis Type 2 35 0.048
112
SVN001 Sveinsson Choreoretinal Atrophy 26 0.048
113
P HYP117 Hypertriglyceridemia 65 0.046
114
LPD008 Lipid Metabolism Disorder 58 0.046
115
P CHN012 Chondrosarcoma 57 0.046
116
EXC002 Exocrine Pancreatic Insufficiency 43 0.046
117
c HMC035 Hemochromatosis, Type 4 39 0.046
118
ADL053 Adult Astrocytic Tumour 37 0.046
119
MDS018 Mediastinal Cancer 36 0.046
120
ALK003 Aleukemic Leukemia Cutis 31 0.046
121
DFF007 Diffuse Infiltrative Lymphocytosis Syndrome 31 0.046
122
c ACT219 Acute Myeloid Leukemia, Flt3-Related 31 0.046
123
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 30 0.046
124
c ACT194 Acute Myeloid Leukemia with T(8;21)(q22;q22) Translocation 29 0.046
125
CLV004 Calvarial Hyperostosis 28 0.046
126
P ALG002 Alagille Syndrome 72 0.042
127
TTR001 Tetralogy of Fallot 71 0.042
128
LPP001 Lipoprotein Lipase Deficiency 65 0.042
129
P PRD006 Prader-Willi Syndrome 63 0.042
130
TNG002 Tangier Disease 61 0.042
131
HJD001 Hajdu-Cheney Syndrome 58 0.042
132
INT079 Intrahepatic Cholangiocarcinoma 55 0.042
133
P OLG002 Oligodendroglioma 55 0.042
134
NNT012 Neonatal Jaundice 51 0.042
135
P FML035 Familial Hyperlipidemia 50 0.042
136
CDS001 Cadasil 50 0.042
137
P GLM040 Glioma Susceptibility 1 48 0.042
138
P HYP090 Hyperalphalipoproteinemia 46 0.042
139
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 46 0.042
140
LPP002 Lipoprotein Glomerulopathy 46 0.042
141
FBR008 Fibrillary Astrocytoma 46 0.042
142
c CHL082 Cholestasis, Progressive Familial Intrahepatic 3 46 0.042
143
c CHL120 Cholestasis, Benign Recurrent Intrahepatic 45 0.042
144
P D2H001 D-2-Hydroxyglutaric Aciduria 44 0.042
145
HMZ003 Homozygous Familial Hypercholesterolemia 44 0.042
146
c CHL081 Cholestasis, Progressive Familial Intrahepatic 2 43 0.042
147
P ATR010 Atrial Heart Septal Defect 43 0.042
148
ICH002 Ichthyosis Bullosa of Siemens 43 0.042
149
FSH001 Fish-Eye Disease 43 0.042
150
P OSS001 Ossifying Fibroma 42 0.042
151
HYP081 Hypolipoproteinemia 41 0.042
152
ANP009 Anaplastic Oligodendroglioma 41 0.042
153
MLT145 Multiple Enchondromatosis, Maffucci Type 40 0.042
154
DRG001 Drug Psychosis 40 0.042
155
TRC021 Tricuspid Valve Stenosis 39 0.042
156
c AMY009 Amyloidosis Aa 39 0.042
157
ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 38 0.042
158
c ADL008 Adult Oligodendroglioma 37 0.042
159
PLC004 Pilocytic Astrocytoma of Cerebellum 36 0.042
160
INT025 Intermittent Explosive Disorder 36 0.042
161
BRS032 Breast Papillary Carcinoma 35 0.042
162
ARC001 Arcus Senilis 35 0.042
163
INT016 Intraductal Papilloma 32 0.042
164
FML330 Familial Lcat Deficiency 32 0.042
165
DRG004 Drug-Induced Mental Disorder 32 0.042
166
CHN003 Chondroblastic Osteosarcoma 31 0.042
167
CHR355 Chromosome 15q13.3 Microdeletion Syndrome 30 0.042
168
SPN012 Spindle Cell Hemangioma 30 0.042
169
c HMC034 Hemochromatosis, Type 5 29 0.042
170
OSM001 Osmotic Diarrhea 29 0.042
171
P 2HY001 2-Hydroxyglutaric Aciduria 28 0.042
172
ENC014 Enchondroma 28 0.042
173
TNM002 Tinea Manuum 24 0.042
174
LWG002 Low Gamma-Gt Familial Intrahepatic Cholestasis 24 0.042
175
INT033 Intracranial Chondrosarcoma 22 0.042
176
APD001 Apo a-I Deficiency 20 0.042
177
INT012 Interval Angle-Closure Glaucoma 20 0.042
178
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 13 0.042
179
P PBL002 Piebald Trait, Kit-Related 7 0.042