Search results for "dyserythropoietic anemia"

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

173 hits were found for 'dyserythropoietic anemia'

# Family MCID Name MIFTS Score
1
c DYS170 Dyserythropoietic Anemia, Congenital, Type Ii 29 8.677
2
c DYS156 Dyserythropoietic Anemia, Congenital, Type Ia 35 8.577
3
P CNG003 Congenital Dyserythropoietic Anemia 38 7.334
4
c DYS168 Dyserythropoietic Anemia, Congenital, Type Iv 25 7.096
5
c DYS167 Dyserythropoietic Anemia, Congenital, Type Iii 24 6.774
6
c DYS155 Dyserythropoietic Anemia, Congenital, Type Ib 23 5.251
7
THR097 Thrombocytopenia, X-Linked, with or Without Dyserythropoietic Anemia 19 5.247
8
EXC004 Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis 22 4.906
9
MJD001 Majeed Syndrome 32 4.782
10
DYS127 Dyserythropoietic Anemia and Thrombocytopenia 17 3.892
11
THR108 Thrombocytopenia with or Without Dyserythropoietic Anemia 12 3.755
12
GT1003 Gata1-Related Anemia with Thrombocytopenia 3 2.391
13
CRN237 Corneal Dystrophy, Avellino Type 31 2.332
14
GT1004 Gata1-Related Cytopenia 5 2.168
15
THL011 Thalassemia-Beta, Dominant Inclusion-Body 22 2.127
16
P HML002 Hemolytic Anemia 60 0.418
17
DFC004 Deficiency Anemia 64 0.371
18
IRN001 Iron Deficiency Anemia 51 0.287
19
P LKM002 Leukemia 70 0.239
20
P THL005 Thalassemia 61 0.219
21
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.207
22
P THR014 Thrombocytopenia 63 0.196
23
P SDR003 Sideroblastic Anemia 40 0.193
24
MCR017 Macrocytic Anemia 43 0.192
25
MYL009 Myelodysplastic Syndrome 73 0.188
26
c CNG027 Congenital Hemolytic Anemia 46 0.187
27
P HMC003 Hemochromatosis 71 0.184
28
ALR002 Al-Raqad Syndrome 36 0.182
29
HMT018 Hematopoietic Stem Cell Transplantation 39 0.170
30
HMT002 Hematologic Cancer 62 0.146
31
SPL018 Splenomegaly 45 0.138
32
PYR013 Pyruvate Kinase Deficiency 58 0.137
33
NTR005 Nutritional Deficiency Disease 51 0.132
34
HYD012 Hydrops Fetalis 45 0.132
35
CRB009 Cerebritis 36 0.130
36
P MYL006 Myeloid Leukemia 67 0.129
37
c ACT073 Acute Leukemia 61 0.126
38
CNG034 Congestive Heart Failure 72 0.125
39
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.123
40
HPT074 Hepatic Adenoma, Somatic 35 0.120
41
OST017 Osteomyelitis 60 0.115
42
P DYS007 Dyskeratosis Congenita 64 0.114
43
P LVR013 Liver Disease 76 0.114
44
P PLM037 Pulmonary Hypertension 78 0.111
45
c CNG401 Congenital Heart Disease 67 0.110
46
HRY003 Hairy Cell Leukemia 56 0.109
47
PRP030 Purpura 60 0.107
48
IMM127 Immune System Cancer 41 0.105
49
CHR288 Chronic Recurrent Multifocal Osteomyelitis 45 0.104
50
MDS022 Mediastinitis 37 0.103
51
c LKM061 Leukemia, Acute Myeloid 71 0.098
52
VTM002 Vitamin B12 Deficiency 45 0.096
53
P ANT006 Antiphospholipid Syndrome 60 0.096
54
PRP007 Priapism 48 0.094
55
P PNC044 Pancreatitis 62 0.093
56
THR042 Thrombocytopenia, X-Linked 46 0.092
57
OTP003 Oto-Palatal-Digital Syndrome 14 0.092
58
ACR013 Acrodysostosis 50 0.089
59
P HRD011 Hereditary Spherocytosis 51 0.086
60
ACT098 Acute Erythroid Leukemia 34 0.086
61
P GT001 Gout 58 0.086
62
P SCL018 Scoliosis 56 0.085
63
GT1001 Gata1-Related X-Linked Cytopenia 3 0.085
64
P PLM006 Pulmonary Alveolar Proteinosis 46 0.083
65
RPP001 Rapp-Hodgkin Syndrome 52 0.082
66
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.082
67
ALN001 Aland Island Eye Disease 45 0.081
68
GRN017 Granulocytopenia 39 0.080
69
RTN023 Retinitis 49 0.080
70
CHL068 Cholestasis 57 0.080
71
c CRN214 Coronary Heart Disease 5 22 0.080
72
c PRM225 Primary Thrombocytopenia 42 0.077
73
P CRN178 Coronary Heart Disease 6 22 0.076
74
CHR563 Chronic Eosinophilic Leukemia 46 0.076
75
P ATR010 Atrial Heart Septal Defect 41 0.075
76
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.075
77
DBN001 Dubin-Johnson Syndrome 52 0.074
78
PBL001 Piebaldism 56 0.074
79
FBR032 Fibromuscular Dysplasia 39 0.074
80
ECT006 Ectodermal Dysplasia 46 0.074
81
NRM003 Norum Disease 53 0.074
82
HYP068 Hyperostosis 39 0.074
83
NDL013 Nodular Regenerative Hyperplasia 46 0.072
84
MYL003 Myeloid Sarcoma 48 0.071
85
LKM067 Leukemia, Acute Promyelocytic, Somatic 55 0.069
86
ADP007 Adie Pupil 33 0.069
87
P INT001 Intrahepatic Cholestasis 58 0.069
88
SVN001 Sveinsson Choreoretinal Atrophy 28 0.069
89
ACT113 Acute Myeloblastic Leukemia with Maturation 40 0.069
90
ACT114 Acute Myeloblastic Leukemia Without Maturation 29 0.069
91
HNM002 Hinman Syndrome 22 0.069
92
P GLM045 Glioma 53 0.067
93
KRT002 Keratomalacia 50 0.067
94
c RNL016 Renal Infectious Disease 22 0.067
95
PYR009 Pyridoxine Deficiency Anemia 20 0.066
96
ENC044 Enchondromatosis, Multiple, Ollier Type 44 0.065
97
HYP121 Hypoalphalipoproteinemia 61 0.065
98
P OLG002 Oligodendroglioma 55 0.065
99
GRD007 Grade Iii Astrocytoma 50 0.065
100
c ACT219 Acute Myeloid Leukemia, Flt3-Related 32 0.065
101
DFF007 Diffuse Infiltrative Lymphocytosis Syndrome 32 0.065
102
ADL053 Adult Astrocytic Tumour 36 0.065
103
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 32 0.065
104
c ACT194 Acute Myeloid Leukemia with T(8;21)(q22;q22) Translocation 29 0.065
105
ALK003 Aleukemic Leukemia Cutis 32 0.065
106
ANM026 Anemia, X-Linked, with/without Neutropenia and/or Platelet Abnormalities 21 0.063
107
HDC001 Headache 52 0.063
108
P HYP117 Hypertriglyceridemia 65 0.063
109
P CHN012 Chondrosarcoma 57 0.063
110
CLV004 Calvarial Hyperostosis 29 0.063
111
HYP081 Hypolipoproteinemia 42 0.063
112
EXC002 Exocrine Pancreatic Insufficiency 41 0.063
113
BCL002 B Cell Deficiency 50 0.061
114
ATS010 Autosomal Recessive Disease 40 0.061
115
P ALG002 Alagille Syndrome 70 0.060
116
ICH002 Ichthyosis Bullosa of Siemens 44 0.060
117
TNG002 Tangier Disease 61 0.060
118
P PRD006 Prader-Willi Syndrome 64 0.060
119
HJD001 Hajdu-Cheney Syndrome 60 0.060
120
P HYP614 Hyperlipidemia, Familial Combined 50 0.060
121
P GLM040 Glioma Susceptibility 1 46 0.060
122
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 45 0.060
123
P D2H001 D-2-Hydroxyglutaric Aciduria 45 0.060
124
FSH001 Fish-Eye Disease 44 0.060
125
P AST007 Astrocytoma 66 0.060
126
LPP001 Lipoprotein Lipase Deficiency 63 0.060
127
FML026 Familial Lipoprotein Lipase Deficiency 51 0.060
128
CHR355 Chromosome 15q13.3 Microdeletion Syndrome 34 0.060
129
CNR028 Cone-Rod Dystropy, X-Linked, 3 23 0.060
130
MLT145 Multiple Enchondromatosis, Maffucci Type 48 0.060
131
FBR008 Fibrillary Astrocytoma 43 0.060
132
c NGH020 Night Blindness, Congenital Stationary , 2a, X-Linked 24 0.060
133
P HYP090 Hyperalphalipoproteinemia 45 0.060
134
CDS001 Cadasil 50 0.060
135
ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 38 0.060
136
LPP002 Lipoprotein Glomerulopathy 46 0.060
137
TNM002 Tinea Manuum 23 0.060
138
P FML035 Familial Hyperlipidemia 49 0.060
139
INT079 Intrahepatic Cholangiocarcinoma 55 0.060
140
TRC021 Tricuspid Valve Stenosis 37 0.060
141
P 2HY001 2-Hydroxyglutaric Aciduria 29 0.060
142
c ADL008 Adult Oligodendroglioma 34 0.060
143
P OSS001 Ossifying Fibroma 43 0.060
144
GMS001 Gemistocytic Astrocytoma 39 0.060
145
SPN012 Spindle Cell Hemangioma 31 0.060
146
INT025 Intermittent Explosive Disorder 35 0.060
147
ARC001 Arcus Senilis 36 0.060
148
INT016 Intraductal Papilloma 32 0.060
149
DRG001 Drug Psychosis 39 0.060
150
ANP009 Anaplastic Oligodendroglioma 37 0.060
151
BRS032 Breast Papillary Carcinoma 35 0.060
152
INT012 Interval Angle-Closure Glaucoma 19 0.060
153
PLC004 Pilocytic Astrocytoma of Cerebellum 32 0.060
154
CHN003 Chondroblastic Osteosarcoma 38 0.060
155
GRN006 Granulomatous Angiitis 42 0.060
156
OSM001 Osmotic Diarrhea 28 0.060
157
DRG004 Drug-Induced Mental Disorder 31 0.060
158
ENC014 Enchondroma 27 0.060
159
HMZ003 Homozygous Familial Hypercholesterolemia 43 0.060
160
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 14 0.060
161
INT033 Intracranial Chondrosarcoma 22 0.060
162
APD001 Apo a-I Deficiency 18 0.060
163
P PBL002 Piebald Trait, Kit-Related 8 0.060
164
RNL007 Renal Tubular Acidosis 50 0.059
165
c CRN177 Coronary Heart Disease 7 21 0.058
166
c TRC078 Trichohepatoenteric Syndrome 2 30 0.056
167
ATS009 Autosomal Genetic Disease 38 0.055
168
c HMC010 Hemochromatosis, Type 3 38 0.053
169
BNF002 Bone Fracture 46 0.051
170
c HMC035 Hemochromatosis, Type 4 38 0.049
171
c HMC009 Hemochromatosis Type 2 30 0.049
172
NNT012 Neonatal Jaundice 49 0.046
173
c HMC034 Hemochromatosis, Type 5 28 0.043