Search results for "elliptocytosis"

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

92 hits were found for 'elliptocytosis'

# Family MCID Name MIFTS Score
1
P HRD012 Hereditary Elliptocytosis 58 8.300
2
c ELL006 Elliptocytosis 3 15 5.270
3
c ELL005 Elliptocytosis 2 15 4.713
4
ALP070 Alport Syndrome - Intellectual Disability - Midface Hypoplasia - Elliptocytosis 24 4.082
5
OVL001 Ovalocytosis, Southeast Asian 17 3.399
6
ALP035 Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis 12 3.399
7
P PYR011 Pyropoikilocytosis 32 0.234
8
P HRD011 Hereditary Spherocytosis 62 0.196
9
ALP004 Alport Syndrome 60 0.150
10
P HML002 Hemolytic Anemia 66 0.139
11
P MLR004 Malaria 75 0.127
12
MNT147 Mental Retardation 51 0.127
13
c THL005 Thalassemia 72 0.113
14
c BTT002 Beta Thalassemia 77 0.098
15
c HPT021 Hepatitis 64 0.098
16
P RNL007 Renal Tubular Acidosis 57 0.098
17
P ATX002 Ataxia Telangiectasia 86 0.080
18
INF030 Infectious Mononucleosis 84 0.080
19
c TXP001 Toxoplasmosis 65 0.080
20
c VRL010 Viral Hepatitis 64 0.080
21
c HPT003 Hepatitis a 59 0.080
22
P CNG021 Congenital Toxoplasmosis 57 0.080
23
PLS007 Plasmodium Falciparum Malaria 55 0.080
24
ART001 Arterial Tortuosity Syndrome 54 0.080
25
AND003 Andersen-Tawil Syndrome 53 0.080
26
P ATS015 Autosomal Dominant Alport Syndrome 52 0.080
27
HMG005 Hemoglobinopathy 51 0.080
28
CHL004 Cholelithiasis 47 0.080
29
VTM002 Vitamin B12 Deficiency 46 0.080
30
c PYR017 Pyropoikilocytosis Hereditary 15 0.080
31
c PRM152 Primary Renal Tubular Acidosis 11 0.080
32
c ELL007 Elliptocytosis-1 9 0.080
33
AND002 Androgen Insensitivity Syndrome 80 0.057
34
ANK002 Ankylosing Spondylitis 74 0.057
35
KWS002 Kawasaki Disease 73 0.057
36
c PRM002 Primary Hyperoxaluria 72 0.057
37
P PND002 Pendred Syndrome 70 0.057
38
P ANG001 Angelman Syndrome 70 0.057
39
ACN002 Acanthosis Nigricans 69 0.057
40
PRT014 Protein S Deficiency 67 0.057
41
CHR452 Chorea-Acanthocytosis 67 0.057
42
c AXN002 Axenfeld-Rieger Syndrome 66 0.057
43
EXT034 Extrinsic Allergic Alveolitis 65 0.057
44
PLS006 Plasmodium Vivax Malaria 65 0.057
45
P HRD057 Hereditary Pancreatitis 64 0.057
46
ART019 Aortic Valve Stenosis 64 0.057
47
P HMP002 Hemophagocytic Lymphohistiocytosis 63 0.057
48
STF001 Stiff-Person Syndrome 63 0.057
49
LRN003 Learning Disability 62 0.057
50
DFC004 Deficiency Anemia 62 0.057
51
P HYP098 Hypereosinophilic Syndrome 61 0.057
52
PRP007 Priapism 60 0.057
53
P ALP006 Alpha Thalassemia 58 0.057
54
MYC002 Mycobacterium Avium Complex Disease 58 0.057
55
HYP063 Hypersplenism 58 0.057
56
PRT039 Proteinuria 57 0.057
57
PTN002 Patent Ductus Arteriosus 57 0.057
58
SNS001 Sensorineural Hearing Loss 57 0.057
59
P HRM005 Hermansky-Pudlak Syndrome 1 53 0.057
60
c HRM001 Hermansky-Pudlak Syndrome 53 0.057
61
c ACR001 Aicardi-Goutieres Syndrome 53 0.057
62
HNT002 Hantavirus Pulmonary Syndrome 53 0.057
63
PRN011 Pernicious Anemia 53 0.057
64
c KRN004 Kernicterus 52 0.057
65
THR013 Thoracic Outlet Syndrome 52 0.057
66
P STR020 Strabismus 51 0.057
67
MNN014 Mononeuritis 51 0.057
68
MLK003 Melkersson-Rosenthal Syndrome 50 0.057
69
P INT063 Intellectual Disability 50 0.057
70
ACN014 Acanthocytosis 48 0.057
71
GLC009 Glucosephosphate Dehydrogenase Deficiency 47 0.057
72
NRN002 Neuronitis 43 0.057
73
RPP001 Rapp-Hodgkin Syndrome 43 0.057
74
P ATX010 Ataxia Neuropathy Spectrum 41 0.057
75
HYP265 Hypotonia 41 0.057
76
c MYP006 Myopia 40 0.057
77
c MLR021 Malaria, Severe 38 0.057
78
c SPH018 Spherocytosis, Hereditary, Type 5 38 0.057
79
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 37 0.057
80
SML020 Small Patella Syndrome 35 0.057
81
XLN009 X-Linked Spinal-Bulbar Muscle Atrophy 33 0.057
82
SYN053 Syndromic Diarrhea 32 0.057
83
P MYP018 Myopia 6 30 0.057
84
TFT003 Tufting Enteropathy 28 0.057
85
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.057
86
BLD052 Blood Group Incompatibility 28 0.057
87
SPN066 Spinal-Bulbar Muscular Atrophy 27 0.057
88
c RNL045 Renal Tubular Acidosis, Distal 27 0.057
89
P RNL066 Renal Tubular Acidosis, Distal, Ad 26 0.057
90
c BNG076 Benign Exophthalmos Syndrome 22 0.057
91
AND005 Androgen Insensitivity Syndrome, Mild 21 0.057
92
RHM007 Rheumatic Congestive Heart Failure 20 0.057