Search results for homozygous hereditary elliptocytosis

37 hits were found for homozygous hereditary elliptocytosis

# Family MCID Name MIFTS Score
1
P HRD012 Hereditary Elliptocytosis 41 0.644
2
P HRD011 Hereditary Spherocytosis 55 0.309
3
P THL005 Thalassemia 65 0.227
4
c BLD140 Blood Group, I System 37 0.209
5
PYR040 Pyropoikilocytosis, Hereditary 35 0.203
6
THR024 Thrombosis 61 0.188
7
c ELL005 Elliptocytosis 2 29 0.187
8
P HML002 Hemolytic Anemia 62 0.187
9
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.186
10
P HPT021 Hepatitis 75 0.171
11
RTN023 Retinitis 52 0.164
12
OVL001 Ovalocytosis, Southeast Asian 30 0.163
13
CRB009 Cerebritis 41 0.157
14
AGN016 Aging 65 0.157
15
c BTT014 Beta-Thalassemia 70 0.155
16
P ANR048 Aniridia 1 68 0.151
17
ANR038 Anorexia Nervosa 1 21 0.145
18
BLD137 Blood Group--Ahonen 17 0.145
19
ALP046 Alport Syndrome, X-Linked 74 0.136
20
P LKM002 Leukemia 75 0.123
21
P RNL007 Renal Tubular Acidosis 51 0.119
22
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.107
23
HMG005 Hemoglobinopathy 53 0.095
24
P FML018 Familial Mediterranean Fever 73 0.093
25
CHL004 Cholelithiasis 51 0.085
26
BRC012 Brucellosis 71 0.084
27
HYP063 Hypersplenism 49 0.080
28
P HMG032 Hemoglobin H Disease 53 0.078
29
P RNL045 Renal Tubular Acidosis, Distal 42 0.076
30
VTM002 Vitamin B12 Deficiency 46 0.075
31
P MYL006 Myeloid Leukemia 69 0.072
32
c SPH013 Spherocytosis, Type 1 53 0.070
33
NPH003 Nephrocalcinosis 49 0.064
34
GLC009 Glucosephosphate Dehydrogenase Deficiency 48 0.063
35
ATH013 Atherosclerosis Susceptibility 59 0.053
36
ART001 Arterial Tortuosity Syndrome 53 0.053
37
HYP458 Hyper Ige Syndrome 46 0.053
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