Search results for "elliptocytosis"

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

93 hits were found for 'elliptocytosis'

# Family MCID Name MIFTS Score
1
P HRD012 Hereditary Elliptocytosis 57 7.505
2
c ELL006 Elliptocytosis 3 16 4.955
3
c ELL005 Elliptocytosis 2 16 4.437
4
ALP070 Alport Syndrome - Intellectual Disability - Midface Hypoplasia - Elliptocytosis 26 3.819
5
HMZ002 Homozygous Hereditary Elliptocytosis 21 3.318
6
c CMM019 Common Hereditary Elliptocytosis 10 3.237
7
OVL001 Ovalocytosis, Southeast Asian 17 3.185
8
ALP035 Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis 12 3.185
9
c ELL007 Elliptocytosis-1 12 2.319
10
P PYR011 Pyropoikilocytosis 37 0.249
11
P HRD011 Hereditary Spherocytosis 68 0.214
12
c HML002 Hemolytic Anemia 65 0.151
13
P ALP004 Alport Syndrome 63 0.151
14
c MNT147 Mental Retardation 56 0.128
15
P MLR004 Malaria 74 0.114
16
c THL005 Thalassemia 71 0.114
17
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 43 0.114
18
c BTT002 Beta Thalassemia 82 0.099
19
c HPT021 Hepatitis 63 0.099
20
RNL007 Renal Tubular Acidosis 56 0.099
21
MNN014 Mononeuritis 51 0.099
22
SYN053 Syndromic Diarrhea 34 0.099
23
c PYR017 Pyropoikilocytosis Hereditary 15 0.099
24
P ATX002 Ataxia Telangiectasia 87 0.081
25
INF030 Infectious Mononucleosis 84 0.081
26
ANK002 Ankylosing Spondylitis 76 0.081
27
P FML018 Familial Mediterranean Fever 75 0.081
28
P ANG001 Angelman Syndrome 71 0.081
29
c TXP001 Toxoplasmosis 65 0.081
30
c VRL010 Viral Hepatitis 63 0.081
31
ART019 Aortic Valve Stenosis 63 0.081
32
DFC004 Deficiency Anemia 62 0.081
33
c HPT003 Hepatitis a 58 0.081
34
P CNG021 Congenital Toxoplasmosis 57 0.081
35
PLS007 Plasmodium Falciparum Malaria 56 0.081
36
ART001 Arterial Tortuosity Syndrome 55 0.081
37
c ATS015 Autosomal Dominant Alport Syndrome 54 0.081
38
AND003 Andersen-Tawil Syndrome 53 0.081
39
THR013 Thoracic Outlet Syndrome 52 0.081
40
HMG005 Hemoglobinopathy 51 0.081
41
CHL004 Cholelithiasis 47 0.081
42
VTM002 Vitamin B12 Deficiency 47 0.081
43
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 29 0.081
44
TFT003 Tufting Enteropathy 28 0.081
45
AND002 Androgen Insensitivity Syndrome 80 0.057
46
KWS002 Kawasaki Disease 75 0.057
47
P ALP006 Alpha Thalassemia 74 0.057
48
c PRM002 Primary Hyperoxaluria 73 0.057
49
P PND002 Pendred Syndrome 71 0.057
50
c AXN002 Axenfeld-Rieger Syndrome 69 0.057
51
CHR452 Chorea-Acanthocytosis 67 0.057
52
PLS006 Plasmodium Vivax Malaria 66 0.057
53
STF001 Stiff-Person Syndrome 66 0.057
54
ACN002 Acanthosis Nigricans 64 0.057
55
P HRD057 Hereditary Pancreatitis 64 0.057
56
LRN003 Learning Disability 62 0.057
57
P HYP098 Hypereosinophilic Syndrome 61 0.057
58
PRP007 Priapism 59 0.057
59
c HMP002 Hemophagocytic Lymphohistiocytosis 59 0.057
60
MYC002 Mycobacterium Avium Complex Disease 58 0.057
61
P HRM005 Hermansky-Pudlak Syndrome 1 58 0.057
62
KNN001 Kennedy's Disease 58 0.057
63
HYP063 Hypersplenism 58 0.057
64
PTN002 Patent Ductus Arteriosus 57 0.057
65
PRT039 Proteinuria 57 0.057
66
SNS001 Sensorineural Hearing Loss 57 0.057
67
c HRM001 Hermansky-Pudlak Syndrome 54 0.057
68
c ACR001 Aicardi-Goutieres Syndrome 54 0.057
69
HNT002 Hantavirus Pulmonary Syndrome 52 0.057
70
c KRN004 Kernicterus 51 0.057
71
MLK003 Melkersson-Rosenthal Syndrome 51 0.057
72
P STR020 Strabismus 51 0.057
73
RPP001 Rapp-Hodgkin Syndrome 50 0.057
74
GLC009 Glucosephosphate Dehydrogenase Deficiency 50 0.057
75
ACN014 Acanthocytosis 48 0.057
76
P ATX010 Ataxia Neuropathy Spectrum 47 0.057
77
NRN002 Neuronitis 43 0.057
78
c MYP006 Myopia 41 0.057
79
HYP265 Hypotonia 40 0.057
80
SML020 Small Patella Syndrome 38 0.057
81
c MLR021 Malaria, Severe 38 0.057
82
c FML162 Familial Mediterranean Fever, Ad 37 0.057
83
P MYP018 Myopia 6 36 0.057
84
XLN009 X-Linked Spinal-Bulbar Muscle Atrophy 34 0.057
85
P RNL066 Renal Tubular Acidosis, Distal, Ad 32 0.057
86
c RNL045 Renal Tubular Acidosis, Distal 28 0.057
87
BLD052 Blood Group Incompatibility 27 0.057
88
SYN057 Syndromic Intellectual Disability 23 0.057
89
c BNG076 Benign Exophthalmos Syndrome 22 0.057
90
RHM007 Rheumatic Congestive Heart Failure 21 0.057
91
AND005 Androgen Insensitivity Syndrome, Mild 21 0.057
92
ANM026 Anemia, X-Linked, with/without Neutropenia and/or Platelet Abnormalities 17 0.057
93
P INT105 Intellectual Disability Multi-Gene Panels 16 0.057