Search results for "elliptocytosis"

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

73 hits were found for 'elliptocytosis'

# Family MCID Name MIFTS Score
1
c HRD012 Hereditary Elliptocytosis 42 8.051
2
P ELL007 Elliptocytosis-1 22 5.951
3
c ELL006 Elliptocytosis 3 27 5.918
4
c ELL008 Elliptocytosis-2 24 5.424
5
OVL004 Ovalocytosis, Hereditary Hemolytic 21 5.367
6
ALP035 Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis 23 4.878
7
PYR011 Pyropoikilocytosis 35 0.271
8
P HRD011 Hereditary Spherocytosis 51 0.227
9
P HML002 Hemolytic Anemia 60 0.182
10
MLR004 Malaria 80 0.148
11
P ALP004 Alport Syndrome 68 0.148
12
P THL005 Thalassemia 61 0.135
13
P HPT021 Hepatitis 74 0.121
14
RNL007 Renal Tubular Acidosis 50 0.121
15
PLS007 Plasmodium Falciparum Malaria 56 0.105
16
c HPT003 Hepatitis a 55 0.105
17
P TXP001 Toxoplasmosis 61 0.105
18
c VRL010 Viral Hepatitis 60 0.105
19
HMG005 Hemoglobinopathy 49 0.105
20
c CNG021 Congenital Toxoplasmosis 46 0.105
21
CHL004 Cholelithiasis 48 0.105
22
VTM002 Vitamin B12 Deficiency 45 0.105
23
P OST005 Osteogenesis Imperfecta 68 0.086
24
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 49 0.086
25
P EHL033 Ehlers-Danlos Syndrome, Classic Type 55 0.086
26
P KRB001 Krabbe Disease 68 0.086
27
c INF069 Infantile Neuroaxonal Dystrophy 1 44 0.086
28
MHR001 Mohr-Tranebjaerg Syndrome 43 0.086
29
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.086
30
P AND016 Andersen Syndrome 57 0.086
31
c OST135 Osteogenesis Imperfecta, Type I 54 0.086
32
c EHL032 Ehlers-Danlos Syndrome, Type Viib 48 0.086
33
CFF003 Caffey Disease 50 0.086
34
c OST122 Osteogenesis Imperfecta, Type Iii 57 0.086
35
RPP001 Rapp-Hodgkin Syndrome 52 0.086
36
c MNN044 Mannosidosis, Beta 44 0.086
37
c PRK027 Parkinson Disease 15, Autosomal Recessive 43 0.086
38
P EHL001 Ehlers-Danlos Syndrome 61 0.086
39
ART001 Arterial Tortuosity Syndrome 51 0.086
40
MLK003 Melkersson-Rosenthal Syndrome 52 0.086
41
JNS003 Jensen Syndrome 33 0.086
42
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.086
43
c OST080 Osteogenesis Imperfecta, Type Ii 50 0.086
44
SML020 Small Patella Syndrome 36 0.086
45
c OST121 Osteogenesis Imperfecta, Type Iv 46 0.086
46
OST015 Osteochondrodysplasia 54 0.086
47
SNS001 Sensorineural Hearing Loss 52 0.086
48
P SCL018 Scoliosis 56 0.086
49
P DNT011 Dentinogenesis Imperfecta 42 0.086
50
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 32 0.086
51
P INT063 Intellectual Disability 46 0.086
52
NNS032 Non-Syndromic X-Linked Intellectual Disability 30 0.086
53
c LRS002 Larsen-Like Syndrome 38 0.086
54
ANG016 Angiokeratoma 43 0.086
55
ALR002 Al-Raqad Syndrome 36 0.086
56
SPL018 Splenomegaly 45 0.086
57
P GLM007 Glomerulonephritis 56 0.086
58
CL1004 Col1a1/2-Related Osteogenesis Imperfecta 27 0.086
59
P BRC015 Bruck Syndrome 44 0.086
60
SYN057 Syndromic Intellectual Disability 23 0.086
61
P NRX001 Neuroaxonal Dystrophy 32 0.086
62
PRN052 Perinatally Lethal Osteogenesis Imperfecta 26 0.086
63
EHL036 Ehlers-Danlos/osteogenesis Imperfecta Syndrome 22 0.086
64
BND014 Bone Development Disease 40 0.086
65
HGH023 High Bone Mass Osteogenesis Imperfecta 24 0.086
66
c EHL041 Ehlers-Danlos Syndrome, Type Vii 29 0.086
67
NNS031 Non-Syndromic Intellectual Disability 22 0.086
68
c NRD011 Neurodegeneration with Brain Iron Accumulation Disorders 21 0.086
69
RNL101 Renal Cell Carcinoma, Papillary 63 0.061
70
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 77 0.061
71
ANM026 Anemia, X-Linked, with/without Neutropenia and/or Platelet Abnormalities 21 0.061
72
c SPH013 Spherocytosis, Type 1 27 0.061
73
HYP063 Hypersplenism 49 0.061