Search results for common hereditary elliptocytosis

52 hits were found for common hereditary elliptocytosis

# Family MCID Name MIFTS Score
1
P HRD012 Hereditary Elliptocytosis 41 0.631
2
P HRD011 Hereditary Spherocytosis 55 0.310
3
c BLD140 Blood Group, I System 37 0.201
4
P HPT021 Hepatitis 75 0.194
5
AGN016 Aging 65 0.191
6
c ELL005 Elliptocytosis 2 29 0.181
7
P THL005 Thalassemia 65 0.180
8
P HML002 Hemolytic Anemia 62 0.174
9
P ANR048 Aniridia 1 68 0.162
10
ANR038 Anorexia Nervosa 1 21 0.160
11
BLD137 Blood Group--Ahonen 17 0.160
12
THR024 Thrombosis 61 0.159
13
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.157
14
OVL001 Ovalocytosis, Southeast Asian 30 0.156
15
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.156
16
CRB009 Cerebritis 41 0.155
17
P LKM002 Leukemia 75 0.148
18
ALP046 Alport Syndrome, X-Linked 74 0.143
19
MLR004 Malaria 86 0.138
20
RTN023 Retinitis 52 0.134
21
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.121
22
c BTT014 Beta-Thalassemia 70 0.117
23
P RNL007 Renal Tubular Acidosis 51 0.108
24
ALR002 Al-Raqad Syndrome 30 0.108
25
CHL004 Cholelithiasis 51 0.107
26
P FML018 Familial Mediterranean Fever 73 0.093
27
BRC012 Brucellosis 71 0.087
28
P MYL006 Myeloid Leukemia 69 0.086
29
HMG005 Hemoglobinopathy 53 0.083
30
P HMG032 Hemoglobin H Disease 53 0.081
31
DFC004 Deficiency Anemia 62 0.080
32
c HPT003 Hepatitis a 63 0.078
33
P TXP001 Toxoplasmosis 65 0.076
34
PLS007 Plasmodium Falciparum Malaria 59 0.074
35
SPL018 Splenomegaly 45 0.073
36
VTM002 Vitamin B12 Deficiency 46 0.072
37
HYP063 Hypersplenism 49 0.071
38
c VRL010 Viral Hepatitis 59 0.071
39
c CNG021 Congenital Toxoplasmosis 57 0.067
40
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 46 0.067
41
THR004 Thrombocytosis 55 0.066
42
P RNL045 Renal Tubular Acidosis, Distal 42 0.064
43
GLC009 Glucosephosphate Dehydrogenase Deficiency 48 0.064
44
c SPH013 Spherocytosis, Type 1 53 0.063
45
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.061
46
NPH003 Nephrocalcinosis 49 0.060
47
RPP001 Rapp-Hodgkin Syndrome 51 0.056
48
ATH013 Atherosclerosis Susceptibility 59 0.053
49
VGN019 Vaginal Discharge 34 0.053
50
ART001 Arterial Tortuosity Syndrome 53 0.051
51
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 59 0.049
52
HYP458 Hyper Ige Syndrome 46 0.049
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