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

119 hits were found for 'elliptocytosis'

# Family MCID Name MIFTS Score
1
HRD012 Hereditary Elliptocytosis 57 7.901
2
c ELL006 Elliptocytosis 3 11 5.001
3
P ELL005 Elliptocytosis 2 20 4.708
4
SPH019 Spherocytic Elliptocytosis 14 4.520
5
HMZ002 Homozygous Hereditary Elliptocytosis 21 3.927
6
ALP058 Alport Syndrome - Intellectual Deficit - Midface Hypoplasia - Elliptocytosis 25 3.874
7
ALP035 Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis 10 3.378
8
c ELL007 Elliptocytosis-1 21 2.495
9
c RNL045 Renal Tubular Acidosis, Distal 23 0.235
10
P HRD011 Hereditary Spherocytosis 66 0.223
11
ACN014 Acanthocytosis 32 0.203
12
PYR017 Pyropoikilocytosis Hereditary 20 0.196
13
VTM002 Vitamin B12 Deficiency 51 0.189
14
P MYP018 Myopia 6 29 0.182
15
ALP004 Alport Syndrome 69 0.166
16
MNN014 Mononeuritis 48 0.157
17
P RNL066 Renal Tubular Acidosis, Distal, Ad 28 0.157
18
P ATX002 Ataxia Telangiectasia 93 0.148
19
c SPH018 Spherocytosis, Hereditary, Type 5 36 0.139
20
RPP001 Rapp-Hodgkin Syndrome 34 0.139
21
PYR011 Pyropoikilocytosis 29 0.139
22
P RNL048 Renal Tubular Acidosis, Distal, Type 3 20 0.139
23
c THL005 Thalassemia 68 0.129
24
P HML002 Hemolytic Anemia 68 0.129
25
P HRM005 Hermansky-Pudlak Syndrome 1 51 0.129
26
P ATM029 Autoimmune Lymphoproliferative Syndrome, Type Ib 46 0.129
27
ANK002 Ankylosing Spondylitis 75 0.117
28
P ALP006 Alpha Thalassemia 75 0.117
29
P MLR004 Malaria 73 0.117
30
P HRD057 Hereditary Pancreatitis 53 0.117
31
c KRN004 Kernicterus 47 0.117
32
TFT003 Tufting Enteropathy 21 0.117
33
c BTT002 Beta Thalassemia 70 0.105
34
EXT034 Extrinsic Allergic Alveolitis 65 0.105
35
c TXP001 Toxoplasmosis 62 0.105
36
STF001 Stiff-Person Syndrome 60 0.105
37
P CNG021 Congenital Toxoplasmosis 54 0.105
38
c ICH041 Ichthyosis, Autosomal Recessive 4b 31 0.105
39
HRL001 Harlequin Type Ichthyosis 22 0.105
40
c HPT021 Hepatitis 75 0.091
41
PLS006 Plasmodium Vivax Malaria 62 0.091
42
c VRL010 Viral Hepatitis 61 0.091
43
P RNL007 Renal Tubular Acidosis 58 0.091
44
HYP063 Hypersplenism 56 0.091
45
THR013 Thoracic Outlet Syndrome 54 0.091
46
c MLR021 Malaria, Severe 49 0.091
47
NNT012 Neonatal Jaundice 46 0.091
48
CHL079 Children's Interstitial Lung Disease 46 0.091
49
ENT001 Enterocele 42 0.091
50
SYN053 Syndromic Diarrhea 42 0.091
51
ERL004 Early Yaws 33 0.091
52
INF030 Infectious Mononucleosis 78 0.074
53
KWS002 Kawasaki Disease 74 0.074
54
ACN002 Acanthosis Nigricans 73 0.074
55
P PND002 Pendred Syndrome 72 0.074
56
PSY004 Psychotic Disorder 69 0.074
57
c ATM006 Autoimmune Lymphoproliferative Syndrome 68 0.074
58
P HMP002 Hemophagocytic Lymphohistiocytosis 66 0.074
59
HYP458 Hyper Ige Syndrome 65 0.074
60
PLS007 Plasmodium Falciparum Malaria 63 0.074
61
ART001 Arterial Tortuosity Syndrome 62 0.074
62
c HPT003 Hepatitis a 60 0.074
63
MYC002 Mycobacterium Avium Complex Disease 57 0.074
64
ATX019 Ataxia with Vitamin E Deficiency 55 0.074
65
HMG005 Hemoglobinopathy 53 0.074
66
INT007 Intermediate Coronary Syndrome 53 0.074
67
CHL004 Cholelithiasis 51 0.074
68
c ACR001 Aicardi-Goutieres Syndrome 49 0.074
69
MLK003 Melkersson-Rosenthal Syndrome 48 0.074
70
c ATS015 Autosomal Dominant Alport Syndrome 46 0.074
71
AND003 Andersen-Tawil Syndrome 43 0.074
72
MNT147 Mental Retardation 35 0.074
73
P CHR104 Chorea 32 0.074
74
SML020 Small Patella Syndrome 30 0.074
75
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.074
76
RHM007 Rheumatic Congestive Heart Failure 21 0.074
77
c PRM152 Primary Renal Tubular Acidosis 7 0.074
78
AND002 Androgen Insensitivity Syndrome 88 0.052
79
P ANG001 Angelman Syndrome 70 0.052
80
c PRM002 Primary Hyperoxaluria 68 0.052
81
ART019 Aortic Valve Stenosis 68 0.052
82
PRT014 Protein S Deficiency 66 0.052
83
DSS009 Disseminated Intravascular Coagulation 66 0.052
84
DFC004 Deficiency Anemia 66 0.052
85
PTN002 Patent Ductus Arteriosus 65 0.052
86
WST001 West Syndrome 64 0.052
87
NRN002 Neuronitis 64 0.052
88
TYP007 Typhoid Fever 63 0.052
89
CHR452 Chorea-Acanthocytosis 62 0.052
90
SCK005 Sickle Cell Disease 62 0.052
91
HRP004 Herpes Zoster 61 0.052
92
c AXN002 Axenfeld-Rieger Syndrome 60 0.052
93
LRN003 Learning Disability 58 0.052
94
HNT002 Hantavirus Pulmonary Syndrome 57 0.052
95
c HRM001 Hermansky-Pudlak Syndrome 57 0.052
96
PRT039 Proteinuria 57 0.052
97
P STR020 Strabismus 56 0.052
98
SNS001 Sensorineural Hearing Loss 56 0.052
99
PRP007 Priapism 55 0.052
100
P HYP098 Hypereosinophilic Syndrome 54 0.052
101
EHR002 Ehrlichiosis 54 0.052
102
PRN011 Pernicious Anemia 52 0.052
103
GLC009 Glucosephosphate Dehydrogenase Deficiency 48 0.052
104
P ATX010 Ataxia Neuropathy Spectrum 44 0.052
105
SPN066 Spinal-Bulbar Muscular Atrophy 44 0.052
106
c MYP006 Myopia 41 0.052
107
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 39 0.052
108
OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 38 0.052
109
EMN001 Emanuel Syndrome 36 0.052
110
XLN009 X-Linked Spinal-Bulbar Muscle Atrophy 34 0.052
111
HYP265 Hypotonia 30 0.052
112
ATS088 Autosomal Dominant Methemoglobinemia 28 0.052
113
PLS008 Plasmodium Malariae Malaria 28 0.052
114
c RNL046 Renal Tubular Acidosis, Distal, Autosomal Dominant 23 0.052
115
P KRN003 Kernicterus Due to Isoimmunization 21 0.052
116
c BNG076 Benign Exophthalmos Syndrome 21 0.052
117
AND005 Androgen Insensitivity Syndrome, Mild 18 0.052
118
P ISC010 Isochromosome Yp 14 0.052
119
OVL001 Ovalocytosis, Southeast Asian 11 0.052