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 42 0.625
2
P HRD011 Hereditary Spherocytosis 51 0.304
3
PYR011 Pyropoikilocytosis 35 0.219
4
P HPT021 Hepatitis 74 0.205
5
P HML002 Hemolytic Anemia 60 0.184
6
P THL005 Thalassemia 61 0.174
7
MLR004 Malaria 80 0.143
8
ALR002 Al-Raqad Syndrome 36 0.142
9
P ALP004 Alport Syndrome 68 0.131
10
CHL004 Cholelithiasis 48 0.120
11
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.115
12
RNL007 Renal Tubular Acidosis 50 0.109
13
PLS007 Plasmodium Falciparum Malaria 56 0.100
14
P TXP001 Toxoplasmosis 61 0.100
15
c HPT003 Hepatitis a 55 0.098
16
c VRL010 Viral Hepatitis 60 0.097
17
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.096
18
HMG005 Hemoglobinopathy 49 0.094
19
P EHL001 Ehlers-Danlos Syndrome 61 0.094
20
P GLM007 Glomerulonephritis 56 0.093
21
SPL018 Splenomegaly 45 0.091
22
VTM002 Vitamin B12 Deficiency 45 0.091
23
P INT063 Intellectual Disability 46 0.088
24
P SCL018 Scoliosis 56 0.087
25
SNS001 Sensorineural Hearing Loss 52 0.086
26
P DNT011 Dentinogenesis Imperfecta 42 0.081
27
c CNG021 Congenital Toxoplasmosis 46 0.081
28
RPP001 Rapp-Hodgkin Syndrome 52 0.075
29
P OST005 Osteogenesis Imperfecta 68 0.072
30
P KRB001 Krabbe Disease 68 0.072
31
P AND016 Andersen Syndrome 57 0.072
32
ANG016 Angiokeratoma 43 0.071
33
SML020 Small Patella Syndrome 36 0.070
34
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 77 0.067
35
RNL101 Renal Cell Carcinoma, Papillary 63 0.064
36
c SPH013 Spherocytosis, Type 1 27 0.059
37
HYP063 Hypersplenism 49 0.057