Search results for "elliptocytosis"

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

91 hits were found for 'elliptocytosis'

# Family MCID Name MIFTS Score
1
P HRD012 Hereditary Elliptocytosis 58 7.516
2
c ELL006 Elliptocytosis 3 15 4.932
3
c ELL005 Elliptocytosis 2 15 4.412
4
ALP070 Alport Syndrome - Intellectual Disability - Midface Hypoplasia - Elliptocytosis 26 3.821
5
HMZ002 Homozygous Hereditary Elliptocytosis 20 3.321
6
c CMM019 Common Hereditary Elliptocytosis 9 3.239
7
OVL001 Ovalocytosis, Southeast Asian 17 3.187
8
ALP035 Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis 12 3.187
9
c ELL007 Elliptocytosis-1 10 2.290
10
P PYR011 Pyropoikilocytosis 35 0.244
11
P HRD011 Hereditary Spherocytosis 67 0.215
12
c HML002 Hemolytic Anemia 66 0.152
13
ALP004 Alport Syndrome 61 0.152
14
MNT147 Mental Retardation 52 0.129
15
P MLR004 Malaria 75 0.115
16
c THL005 Thalassemia 72 0.115
17
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.115
18
c BTT002 Beta Thalassemia 78 0.100
19
c HPT021 Hepatitis 64 0.100
20
RNL007 Renal Tubular Acidosis 57 0.100
21
MNN014 Mononeuritis 51 0.100
22
SYN053 Syndromic Diarrhea 34 0.100
23
c PYR017 Pyropoikilocytosis Hereditary 15 0.100
24
P ATX002 Ataxia Telangiectasia 87 0.081
25
INF030 Infectious Mononucleosis 84 0.081
26
ANK002 Ankylosing Spondylitis 77 0.081
27
P FML018 Familial Mediterranean Fever 76 0.081
28
P ANG001 Angelman Syndrome 70 0.081
29
c TXP001 Toxoplasmosis 66 0.081
30
c VRL010 Viral Hepatitis 64 0.081
31
ART019 Aortic Valve Stenosis 64 0.081
32
DFC004 Deficiency Anemia 63 0.081
33
c HPT003 Hepatitis a 59 0.081
34
P CNG021 Congenital Toxoplasmosis 57 0.081
35
PLS007 Plasmodium Falciparum Malaria 57 0.081
36
ART001 Arterial Tortuosity Syndrome 55 0.081
37
AND003 Andersen-Tawil Syndrome 54 0.081
38
P ATS015 Autosomal Dominant Alport Syndrome 54 0.081
39
THR013 Thoracic Outlet Syndrome 52 0.081
40
HMG005 Hemoglobinopathy 51 0.081
41
CHL004 Cholelithiasis 48 0.081
42
VTM002 Vitamin B12 Deficiency 48 0.081
43
TFT003 Tufting Enteropathy 28 0.081
44
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.081
45
AND002 Androgen Insensitivity Syndrome 80 0.058
46
KWS002 Kawasaki Disease 76 0.058
47
P ALP006 Alpha Thalassemia 75 0.058
48
c PRM002 Primary Hyperoxaluria 74 0.058
49
PLS006 Plasmodium Vivax Malaria 68 0.058
50
c AXN002 Axenfeld-Rieger Syndrome 67 0.058
51
CHR452 Chorea-Acanthocytosis 67 0.058
52
P HRD057 Hereditary Pancreatitis 66 0.058
53
STF001 Stiff-Person Syndrome 64 0.058
54
ACN002 Acanthosis Nigricans 63 0.058
55
LRN003 Learning Disability 63 0.058
56
P HYP098 Hypereosinophilic Syndrome 62 0.058
57
PRP007 Priapism 60 0.058
58
c HMP002 Hemophagocytic Lymphohistiocytosis 60 0.058
59
MYC002 Mycobacterium Avium Complex Disease 59 0.058
60
KNN001 Kennedy's Disease 59 0.058
61
HYP063 Hypersplenism 59 0.058
62
P HRM005 Hermansky-Pudlak Syndrome 1 58 0.058
63
PRT039 Proteinuria 58 0.058
64
SNS001 Sensorineural Hearing Loss 57 0.058
65
PTN002 Patent Ductus Arteriosus 57 0.058
66
c HRM001 Hermansky-Pudlak Syndrome 55 0.058
67
c ACR001 Aicardi-Goutieres Syndrome 54 0.058
68
HNT002 Hantavirus Pulmonary Syndrome 53 0.058
69
c KRN004 Kernicterus 52 0.058
70
P STR020 Strabismus 52 0.058
71
MLK003 Melkersson-Rosenthal Syndrome 51 0.058
72
ACN014 Acanthocytosis 49 0.058
73
GLC009 Glucosephosphate Dehydrogenase Deficiency 48 0.058
74
RPP001 Rapp-Hodgkin Syndrome 47 0.058
75
NRN002 Neuronitis 44 0.058
76
P ATX010 Ataxia Neuropathy Spectrum 43 0.058
77
c MYP006 Myopia 41 0.058
78
HYP265 Hypotonia 41 0.058
79
c MLR021 Malaria, Severe 39 0.058
80
SML020 Small Patella Syndrome 37 0.058
81
c FML162 Familial Mediterranean Fever, Ad 37 0.058
82
P MYP018 Myopia 6 36 0.058
83
XLN009 X-Linked Spinal-Bulbar Muscle Atrophy 33 0.058
84
P RNL066 Renal Tubular Acidosis, Distal, Ad 30 0.058
85
BLD052 Blood Group Incompatibility 28 0.058
86
c RNL045 Renal Tubular Acidosis, Distal 27 0.058
87
c BNG076 Benign Exophthalmos Syndrome 22 0.058
88
SYN057 Syndromic Intellectual Disability 22 0.058
89
RHM007 Rheumatic Congestive Heart Failure 21 0.058
90
AND005 Androgen Insensitivity Syndrome, Mild 21 0.058
91
P INT105 Intellectual Disability Multi-Gene Panels 16 0.058