Search results for "common hereditary elliptocytosis"

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

35 hits were found for 'common hereditary elliptocytosis'

# Family MCID Name MIFTS Score
1
c HRD012 Hereditary Elliptocytosis 42 0.658
2
P HRD011 Hereditary Spherocytosis 54 0.297
3
PYR011 Pyropoikilocytosis 35 0.227
4
P HPT021 Hepatitis 69 0.195
5
P HML002 Hemolytic Anemia 62 0.171
6
P THL005 Thalassemia 64 0.166
7
THR024 Thrombosis 57 0.159
8
MLR004 Malaria 83 0.135
9
P ALP004 Alport Syndrome 69 0.128
10
CHL004 Cholelithiasis 48 0.109
11
ALR002 Al-Raqad Syndrome 36 0.104
12
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.101
13
RNL007 Renal Tubular Acidosis 50 0.100
14
AND005 Androgen Insensitivity Syndrome, Mild 16 0.096
15
DFC004 Deficiency Anemia 64 0.090
16
c HPT003 Hepatitis a 59 0.087
17
c VRL010 Viral Hepatitis 60 0.083
18
HMG005 Hemoglobinopathy 52 0.083
19
P TXP001 Toxoplasmosis 61 0.082
20
PLS007 Plasmodium Falciparum Malaria 55 0.082
21
P GLM007 Glomerulonephritis 59 0.078
22
VTM002 Vitamin B12 Deficiency 45 0.078
23
SNS001 Sensorineural Hearing Loss 57 0.074
24
SPL018 Splenomegaly 44 0.073
25
c CNG021 Congenital Toxoplasmosis 48 0.070
26
P ATX010 Ataxia Neuropathy Spectrum 30 0.068
27
P INT063 Intellectual Disability 49 0.068
28
c SPH013 Spherocytosis, Type 1 41 0.064
29
NPH003 Nephrocalcinosis 48 0.062
30
P PFF001 Pfeiffer Syndrome 73 0.060
31
RPP001 Rapp-Hodgkin Syndrome 48 0.060
32
HYP063 Hypersplenism 48 0.059
33
P AND016 Andersen Syndrome 58 0.057
34
CHK001 Chikungunya 54 0.057
35
SML020 Small Patella Syndrome 36 0.052