Search results for "elliptocytosis"

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

89 hits were found for 'elliptocytosis'

# Family MCID Name MIFTS Score
1
c HRD012 Hereditary Elliptocytosis 49 7.742
2
c ELL006 Elliptocytosis 3 12 5.161
3
c ELL008 Elliptocytosis-2 17 4.601
4
ALP035 Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis 13 4.066
5
P ELL007 Elliptocytosis-1 15 4.043
6
ALP070 Alport Syndrome - Intellectual Disability - Midface Hypoplasia - Elliptocytosis 22 4.019
7
OVL001 Ovalocytosis, Southeast Asian 15 4.019
8
PYR011 Pyropoikilocytosis 35 0.248
9
P HRD011 Hereditary Spherocytosis 56 0.205
10
P ALP004 Alport Syndrome 60 0.151
11
P HML002 Hemolytic Anemia 56 0.151
12
MLR004 Malaria 81 0.127
13
P MNT147 Mental Retardation 46 0.127
14
P THL005 Thalassemia 64 0.114
15
P HPT021 Hepatitis 55 0.099
16
RNL007 Renal Tubular Acidosis 48 0.099
17
P ATX030 Ataxia-Telangiectasia 76 0.081
18
P TXP001 Toxoplasmosis 56 0.081
19
GLC085 Glucose-6-Phosphate Dehydrogenase Deficiency 57 0.081
20
c VRL010 Viral Hepatitis 54 0.081
21
DFC004 Deficiency Anemia 54 0.081
22
P AND016 Andersen Syndrome 54 0.081
23
c HPT003 Hepatitis a 51 0.081
24
c CNG021 Congenital Toxoplasmosis 50 0.081
25
ART001 Arterial Tortuosity Syndrome 48 0.081
26
PLS007 Plasmodium Falciparum Malaria 48 0.081
27
HMG005 Hemoglobinopathy 44 0.081
28
CHL004 Cholelithiasis 40 0.081
29
VTM002 Vitamin B12 Deficiency 40 0.081
30
c ALP073 Alport Syndrome, Autosomal Recessive 40 0.081
31
P TRC086 Trichohepatoenteric Syndrome 1 39 0.081
32
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.081
33
P ALZ034 Alzheimer Disease 100 0.057
34
P PFF001 Pfeiffer Syndrome 74 0.057
35
P PRM002 Primary Hyperoxaluria 68 0.057
36
AND015 Androgen Insensitivity 69 0.057
37
P ANG001 Angelman Syndrome 66 0.057
38
KWS002 Kawasaki Disease 66 0.057
39
P PND002 Pendred Syndrome 62 0.057
40
P HRM001 Hermansky-Pudlak Syndrome 60 0.057
41
P PLM036 Pulmonary Fibrosis 64 0.057
42
PLS006 Plasmodium Vivax Malaria 57 0.057
43
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 64 0.057
44
ACN002 Acanthosis Nigricans 55 0.057
45
P HYP098 Hypereosinophilic Syndrome 55 0.057
46
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.057
47
P ACR001 Aicardi-Goutieres Syndrome 54 0.057
48
LRN003 Learning Disability 53 0.057
49
c PNC108 Pancreatitis, Hereditary 54 0.057
50
STF001 Stiff-Person Syndrome 52 0.057
51
P AGM001 Agammaglobulinemia 59 0.057
52
MYC002 Mycobacterium Avium Complex Disease 51 0.057
53
P FML161 Familial Mediterranean Fever, Ar 51 0.057
54
PRP007 Priapism 51 0.057
55
HYP063 Hypersplenism 50 0.057
56
PTN002 Patent Ductus Arteriosus 49 0.057
57
P AXN010 Axenfeld-Rieger Syndrome, Type 3 50 0.057
58
c SPN225 Spondyloarthropathy 1 48 0.057
59
SNS001 Sensorineural Hearing Loss 48 0.057
60
P KRN004 Kernicterus 46 0.057
61
HNT002 Hantavirus Pulmonary Syndrome 46 0.057
62
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 45 0.057
63
RPP001 Rapp-Hodgkin Syndrome 45 0.057
64
THR013 Thoracic Outlet Syndrome 45 0.057
65
P STR020 Strabismus 44 0.057
66
MLK003 Melkersson-Rosenthal Syndrome 44 0.057
67
PRT039 Proteinuria 43 0.057
68
MNN014 Mononeuritis 43 0.057
69
P MYP006 Myopia 41 0.057
70
SPL018 Splenomegaly 40 0.057
71
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 38 0.057
72
NRN002 Neuronitis 36 0.057
73
P RNL066 Renal Tubular Acidosis, Distal, Ad 35 0.057
74
P HYP265 Hypotonia 34 0.057
75
BLR008 Bilirubin Metabolic Disorder 32 0.057
76
c ART101 Aortic Valve Disease 2 32 0.057
77
RHM028 Rheumatic Heart Disease 32 0.057
78
P ATX010 Ataxia Neuropathy Spectrum 29 0.057
79
TFT003 Tufting Enteropathy 26 0.057
80
GLC009 Glucosephosphate Dehydrogenase Deficiency 25 0.057
81
BLD052 Blood Group Incompatibility 22 0.057
82
c BNG076 Benign Exophthalmos Syndrome 19 0.057
83
SYN057 Syndromic Intellectual Disability 17 0.057
84
AND005 Androgen Insensitivity Syndrome, Mild 17 0.057
85
c SPH013 Spherocytosis, Type 1 17 0.057
86
FML066 Familial Hypersensitivity Pneumonitis 16 0.057
87
P INT105 Intellectual Disability Multi-Gene Panels 15 0.057
88
ANM026 Anemia, X-Linked, with/without Neutropenia and/or Platelet Abnormalities 13 0.057
89
RSP002 Respiratory Syncytial Virus Infectious Disease 21 0.057