Search results for "common hereditary elliptocytosis"

The MalaCard for "common hereditary elliptocytosis" has been retired.
Searching MalaCards for entries containing "common hereditary elliptocytosis"

37 hits were found for 'common hereditary elliptocytosis'

# Family MCID Name MIFTS Score
1
c HRD012 Hereditary Elliptocytosis 41 0.612
2
P HRD011 Hereditary Spherocytosis 53 0.295
3
PYR011 Pyropoikilocytosis 34 0.215
4
P HPT021 Hepatitis 70 0.193
5
P HML002 Hemolytic Anemia 60 0.165
6
P THL005 Thalassemia 61 0.162
7
MLR004 Malaria 79 0.129
8
P ALP004 Alport Syndrome 68 0.122
9
CHL004 Cholelithiasis 48 0.106
10
ALR002 Al-Raqad Syndrome 36 0.100
11
RNL007 Renal Tubular Acidosis 50 0.096
12
DFC004 Deficiency Anemia 65 0.090
13
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.080
14
c VRL010 Viral Hepatitis 61 0.080
15
P TXP001 Toxoplasmosis 60 0.079
16
c HPT003 Hepatitis a 59 0.079
17
c GLL024 Gallbladder Disease 1 38 0.078
18
HMG005 Hemoglobinopathy 50 0.077
19
PLS007 Plasmodium Falciparum Malaria 54 0.077
20
P EHL001 Ehlers-Danlos Syndrome 61 0.076
21
VTM002 Vitamin B12 Deficiency 44 0.075
22
P GLM007 Glomerulonephritis 56 0.075
23
SPL018 Splenomegaly 44 0.071
24
SNS001 Sensorineural Hearing Loss 57 0.070
25
P SCL018 Scoliosis 56 0.067
26
c CNG021 Congenital Toxoplasmosis 46 0.066
27
P INT063 Intellectual Disability 53 0.066
28
P DNT011 Dentinogenesis Imperfecta 42 0.065
29
P ATX010 Ataxia Neuropathy Spectrum 28 0.063
30
c SPH013 Spherocytosis, Type 1 23 0.057
31
HYP063 Hypersplenism 48 0.056
32
P OST005 Osteogenesis Imperfecta 67 0.056
33
RPP001 Rapp-Hodgkin Syndrome 48 0.056
34
P AND016 Andersen Syndrome 58 0.054
35
P KRB001 Krabbe Disease 69 0.053
36
SRC011 Sarcocystosis 29 0.053
37
SML020 Small Patella Syndrome 36 0.049