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

123 hits were found for 'elliptocytosis'

# ++ Fam MCID Name MIFTS Score
1
HRD012 Hereditary Elliptocytosis 52 7.883
2
c ELL006 Elliptocytosis 3 12 5.044
3
c ELL005 Elliptocytosis 2 11 4.707
4
P ELL007 Elliptocytosis-1 22 4.069
5
SPH019 Spherocytic Elliptocytosis 11 3.969
6
ALP058 Alport Syndrome - Intellectual Deficit - Midface Hypoplasia - Elliptocytosis 22 3.874
7
HMZ002 Homozygous Hereditary Elliptocytosis 20 3.391
8
ALP035 Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis 7 3.376
9
PYR017 Pyropoikilocytosis Hereditary 25 0.329
10
PYR011 Pyropoikilocytosis 30 0.255
11
RNL045 Renal Tubular Acidosis, Distal 34 0.238
12
P HRD011 Hereditary Spherocytosis 59 0.220
13
ACN014 Acanthocytosis 43 0.201
14
VTM002 Vitamin B12 Deficiency 35 0.180
15
P MYP018 Myopia 6 23 0.180
16
ANK002 Ankylosing Spondylitis 75 0.164
17
ALP004 Alport Syndrome 55 0.164
18
MNN014 Mononeuritis 40 0.156
19
RNL066 Renal Tubular Acidosis, Distal, Ad 24 0.156
20
ATX002 Ataxia Telangiectasia 81 0.147
21
PRT014 Protein S Deficiency 67 0.137
22
HML002 Hemolytic Anemia 60 0.137
23
RPP001 Rapp-Hodgkin Syndrome 37 0.137
24
c SPH018 Spherocytosis, Hereditary, Type 5 31 0.137
25
RNL048 Renal Tubular Acidosis, Distal, Type 3 19 0.137
26
THL005 Thalassemia 69 0.127
27
THR013 Thoracic Outlet Syndrome 53 0.127
28
P HRM005 Hermansky-Pudlak Syndrome 1 44 0.127
29
c ATM029 Autoimmune Lymphoproliferative Syndrome, Type Ib 33 0.127
30
P MLR004 Malaria 66 0.116
31
PRT011 Protein C Deficiency 59 0.116
32
HRD057 Hereditary Pancreatitis 53 0.116
33
c MNT147 Mental Retardation 51 0.116
34
P KRN004 Kernicterus 46 0.116
35
TFT003 Tufting Enteropathy 26 0.116
36
BTT002 Beta Thalassemia 69 0.104
37
c MLR021 Malaria, Severe 56 0.104
38
EXT034 Extrinsic Allergic Alveolitis 55 0.104
39
STF001 Stiff-Person Syndrome 55 0.104
40
P CNG021 Congenital Toxoplasmosis 48 0.104
41
c ICH041 Ichthyosis, Autosomal Recessive 4b 23 0.104
42
HRL001 Harlequin Type Ichthyosis 20 0.104
43
PRT056 Protein R Deficiency 20 0.104
44
c HPT021 Hepatitis 65 0.090
45
c TXP001 Toxoplasmosis 59 0.090
46
c VRL010 Viral Hepatitis 57 0.090
47
RNL007 Renal Tubular Acidosis 57 0.090
48
PLS006 Plasmodium Vivax Malaria 56 0.090
49
HYP063 Hypersplenism 52 0.090
50
CHL079 Children's Interstitial Lung Disease 39 0.090
51
ENT001 Enterocele 39 0.090
52
c ERL004 Early Yaws 29 0.090
53
PRM152 Primary Renal Tubular Acidosis 12 0.090
54
ACN002 Acanthosis Nigricans 70 0.073
55
KWS002 Kawasaki Disease 69 0.073
56
P ANG001 Angelman Syndrome 67 0.073
57
DFC004 Deficiency Anemia 65 0.073
58
INF030 Infectious Mononucleosis 65 0.073
59
ART019 Aortic Valve Stenosis 64 0.073
60
PSY004 Psychotic Disorder 62 0.073
61
HMP002 Hemophagocytic Lymphohistiocytosis 62 0.073
62
PND002 Pendred Syndrome 60 0.073
63
P ATM006 Autoimmune Lymphoproliferative Syndrome 60 0.073
64
PLS007 Plasmodium Falciparum Malaria 59 0.073
65
c HPT003 Hepatitis a 57 0.073
66
MYC002 Mycobacterium Avium Complex Disease 56 0.073
67
HYP458 Hyper Ige Syndrome 54 0.073
68
c HPT007 Hepatitis E 52 0.073
69
ART001 Arterial Tortuosity Syndrome 52 0.073
70
CHL004 Cholelithiasis 50 0.073
71
INT007 Intermediate Coronary Syndrome 50 0.073
72
P CHR104 Chorea 46 0.073
73
c ACR001 Aicardi-Goutieres Syndrome 46 0.073
74
MLK003 Melkersson-Rosenthal Syndrome 43 0.073
75
P ATS015 Autosomal Dominant Alport Syndrome 43 0.073
76
NNT012 Neonatal Jaundice 42 0.073
77
ATX019 Ataxia with Vitamin E Deficiency 40 0.073
78
AND003 Andersen-Tawil Syndrome 39 0.073
79
SML020 Small Patella Syndrome 26 0.073
80
P DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 23 0.073
81
RHM007 Rheumatic Congestive Heart Failure 19 0.073
82
AND002 Androgen Insensitivity Syndrome 75 0.052
83
WST001 West Syndrome 64 0.052
84
c PRM002 Primary Hyperoxaluria 63 0.052
85
c HPT016 Hepatitis B 62 0.052
86
PTN002 Patent Ductus Arteriosus 61 0.052
87
P HYP098 Hypereosinophilic Syndrome 61 0.052
88
HRP004 Herpes Zoster 60 0.052
89
TYP007 Typhoid Fever 60 0.052
90
DSS009 Disseminated Intravascular Coagulation 59 0.052
91
GLB001 Gilbert Syndrome 59 0.052
92
SCK005 Sickle Cell Disease 58 0.052
93
c AXN002 Axenfeld-Rieger Syndrome 57 0.052
94
c EMR001 Emery-Dreifuss Muscular Dystrophy 56 0.052
95
c HRM001 Hermansky-Pudlak Syndrome 55 0.052
96
SNS001 Sensorineural Hearing Loss 55 0.052
97
LRN003 Learning Disability 54 0.052
98
HNT002 Hantavirus Pulmonary Syndrome 54 0.052
99
GLL031 Guillain-Barr´┐Ż Syndrome 54 0.052
100
CHR452 Chorea-Acanthocytosis 53 0.052
101
P STR020 Strabismus 53 0.052
102
PRN011 Pernicious Anemia 52 0.052
103
PRP007 Priapism 52 0.052
104
P PRT039 Proteinuria 51 0.052
105
BCL002 B Cell Deficiency 50 0.052
106
HMG005 Hemoglobinopathy 47 0.052
107
EHR002 Ehrlichiosis 46 0.052
108
SPN066 Spinal-Bulbar Muscular Atrophy 44 0.052
109
HYP265 Hypotonia 43 0.052
110
CHR101 Char Syndrome 42 0.052
111
GLC009 Glucosephosphate Dehydrogenase Deficiency 41 0.052
112
c MYP006 Myopia 36 0.052
113
EMN001 Emanuel Syndrome 34 0.052
114
c ATX010 Ataxia Neuropathy Spectrum 33 0.052
115
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 29 0.052
116
c OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 29 0.052
117
XLN009 X-Linked Spinal-Bulbar Muscle Atrophy 28 0.052
118
RNL046 Renal Tubular Acidosis, Distal, Autosomal Dominant 25 0.052
119
ATS088 Autosomal Dominant Methemoglobinemia 24 0.052
120
AND005 Androgen Insensitivity Syndrome, Mild 19 0.052
121
c KRN003 Kernicterus Due to Isoimmunization 18 0.052
122
c BNG076 Benign Exophthalmos Syndrome 17 0.052
123
P ISC010 Isochromosome Yp 14 0.052