Search results for "elliptocytosis"

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

79 hits were found for 'elliptocytosis'

# Family MCID Name MIFTS Score
1
c HRD012 Hereditary Elliptocytosis 41 8.008
2
P ELL007 Elliptocytosis-1 22 6.362
3
c ELL006 Elliptocytosis 3 26 6.346
4
OVL004 Ovalocytosis, Hereditary Hemolytic 24 6.293
5
c ELL008 Elliptocytosis-2 30 5.872
6
ALP035 Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis 22 4.867
7
PYR011 Pyropoikilocytosis 34 0.264
8
P HRD011 Hereditary Spherocytosis 53 0.213
9
P HML002 Hemolytic Anemia 60 0.156
10
MLR004 Malaria 79 0.132
11
P ALP004 Alport Syndrome 68 0.132
12
P THL005 Thalassemia 61 0.118
13
P HPT021 Hepatitis 70 0.102
14
RNL007 Renal Tubular Acidosis 50 0.102
15
c VRL010 Viral Hepatitis 61 0.084
16
P TXP001 Toxoplasmosis 60 0.084
17
c HPT003 Hepatitis a 59 0.084
18
PLS007 Plasmodium Falciparum Malaria 54 0.084
19
HMG005 Hemoglobinopathy 50 0.084
20
CHL004 Cholelithiasis 48 0.084
21
c CNG021 Congenital Toxoplasmosis 46 0.084
22
VTM002 Vitamin B12 Deficiency 44 0.084
23
P KRB001 Krabbe Disease 69 0.059
24
P OST005 Osteogenesis Imperfecta 67 0.059
25
DFC004 Deficiency Anemia 65 0.059
26
P ORT004 Orthostatic Intolerance 65 0.059
27
P EHL001 Ehlers-Danlos Syndrome 61 0.059
28
c OST122 Osteogenesis Imperfecta, Type Iii 58 0.059
29
P AND016 Andersen Syndrome 58 0.059
30
SNS001 Sensorineural Hearing Loss 57 0.059
31
P GLM007 Glomerulonephritis 56 0.059
32
P SCL018 Scoliosis 56 0.059
33
c OST135 Osteogenesis Imperfecta, Type I 55 0.059
34
P EHL033 Ehlers-Danlos Syndrome, Classic Type 54 0.059
35
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.059
36
KNS001 Kniest Dysplasia 53 0.059
37
P INT063 Intellectual Disability 53 0.059
38
CFF003 Caffey Disease 53 0.059
39
ART001 Arterial Tortuosity Syndrome 52 0.059
40
c OST080 Osteogenesis Imperfecta, Type Ii 51 0.059
41
MLK003 Melkersson-Rosenthal Syndrome 50 0.059
42
RPP001 Rapp-Hodgkin Syndrome 48 0.059
43
HYP063 Hypersplenism 48 0.059
44
c OST121 Osteogenesis Imperfecta, Type Iv 48 0.059
45
c OST132 Osteogenesis Imperfecta, Type Vi 48 0.059
46
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 48 0.059
47
CRS005 Crest Syndrome 47 0.059
48
c EHL032 Ehlers-Danlos Syndrome, Type Viib 47 0.059
49
P BRC048 Bruck Syndrome 2 45 0.059
50
RFR010 Refractory Anemia 45 0.059
51
c PRK027 Parkinson Disease 15, Autosomal Recessive 44 0.059
52
SPL018 Splenomegaly 44 0.059
53
c MNN044 Mannosidosis, Beta 44 0.059
54
P DNT011 Dentinogenesis Imperfecta 42 0.059
55
c INF069 Infantile Neuroaxonal Dystrophy 1 42 0.059
56
BND014 Bone Development Disease 42 0.059
57
P NRX001 Neuroaxonal Dystrophy 39 0.059
58
c GLL024 Gallbladder Disease 1 38 0.059
59
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 37 0.059
60
HMG025 Hemoglobin H Disease, Nondeletional 37 0.059
61
SML020 Small Patella Syndrome 36 0.059
62
ALR002 Al-Raqad Syndrome 36 0.059
63
c LRS002 Larsen-Like Syndrome 36 0.059
64
c NRD011 Neurodegeneration with Brain Iron Accumulation Disorders 35 0.059
65
JNS003 Jensen Syndrome 34 0.059
66
P RFR008 Refractory Anemia with Excess Blasts 30 0.059
67
SRC011 Sarcocystosis 29 0.059
68
NNS032 Non-Syndromic X-Linked Intellectual Disability 29 0.059
69
c EHL041 Ehlers-Danlos Syndrome, Type Vii 29 0.059
70
P ATX010 Ataxia Neuropathy Spectrum 28 0.059
71
CL1004 Col1a1/2-Related Osteogenesis Imperfecta 26 0.059
72
PRN052 Perinatally Lethal Osteogenesis Imperfecta 25 0.059
73
HGH023 High Bone Mass Osteogenesis Imperfecta 24 0.059
74
ANM026 Anemia, X-Linked, with/without Neutropenia and/or Platelet Abnormalities 24 0.059
75
c SPH013 Spherocytosis, Type 1 23 0.059
76
PRG091 Progressively Deforming Osteogenesis Imperfecta 21 0.059
77
EHL036 Ehlers-Danlos/osteogenesis Imperfecta Syndrome 21 0.059
78
NNS031 Non-Syndromic Intellectual Disability 21 0.059
79
CLS035 Classic Non-Deforming Osteogenesis Imperfecta with Blue Sclerae 20 0.059