Search results for common hereditary elliptocytosis

49 hits were found for common hereditary elliptocytosis

# Family MCID Name MIFTS Score
1
c HRD012 Hereditary Elliptocytosis 41 0.591
2
P HRD011 Hereditary Spherocytosis 53 0.295
3
PYR011 Pyropoikilocytosis 37 0.217
4
P HPT021 Hepatitis 68 0.191
5
P THL005 Thalassemia 61 0.168
6
P HML002 Hemolytic Anemia 61 0.161
7
THR024 Thrombosis 43 0.155
8
P ALP004 Alport Syndrome 70 0.125
9
MLR004 Malaria 82 0.122
10
AND005 Androgen Insensitivity Syndrome, Mild 16 0.112
11
CHL004 Cholelithiasis 47 0.104
12
P LPS004 Lupus Erythematosus 63 0.100
13
ALR002 Al-Raqad Syndrome 29 0.099
14
RNL007 Renal Tubular Acidosis 48 0.094
15
P RHM011 Rheumatoid Arthritis 87 0.092
16
c SYS001 Systemic Lupus Erythematosus 86 0.090
17
c HPT003 Hepatitis a 56 0.079
18
HMG005 Hemoglobinopathy 51 0.078
19
DFC004 Deficiency Anemia 60 0.076
20
c VRL010 Viral Hepatitis 58 0.076
21
P TXP001 Toxoplasmosis 60 0.075
22
VTM002 Vitamin B12 Deficiency 45 0.075
23
P GLM007 Glomerulonephritis 55 0.073
24
PLS007 Plasmodium Falciparum Malaria 54 0.072
25
SPL018 Splenomegaly 45 0.070
26
P LPR003 Leprosy 63 0.067
27
BRC012 Brucellosis 61 0.067
28
SNS001 Sensorineural Hearing Loss 54 0.066
29
P AND016 Andersen Syndrome 59 0.066
30
P ATX010 Ataxia Neuropathy Spectrum 27 0.065
31
P INT063 Intellectual Disability 58 0.064
32
THR004 Thrombocytosis 52 0.064
33
ART001 Arterial Tortuosity Syndrome 51 0.064
34
c CNG021 Congenital Toxoplasmosis 52 0.064
35
PLM001 Pulmonary Tuberculosis 63 0.062
36
P LYM033 Lymphoproliferative Syndrome 54 0.061
37
c SPH013 Spherocytosis, Type 1 42 0.059
38
c ATM006 Autoimmune Lymphoproliferative Syndrome 72 0.058
39
NPH003 Nephrocalcinosis 47 0.058
40
c ATM011 Autoimmune Hepatitis 57 0.057
41
P ALP009 Alopecia Areata 60 0.056
42
P GRV001 Graves' Disease 57 0.055
43
P PFF001 Pfeiffer Syndrome 71 0.054
44
RPP001 Rapp-Hodgkin Syndrome 51 0.054
45
HYP063 Hypersplenism 47 0.053
46
CHK001 Chikungunya 53 0.051
47
STF001 Stiff-Person Syndrome 56 0.051
48
HSH003 Hashimoto Thyroiditis 62 0.049
49
ISC016 Ischiocoxopodopatellar Syndrome 28 0.047
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