Search results for "elliptocytosis"

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

152 hits were found for 'elliptocytosis'

# Family MCID Name MIFTS Score
1
c HRD012 Hereditary Elliptocytosis 42 7.562
2
c ELL006 Elliptocytosis 3 25 5.698
3
P ELL007 Elliptocytosis-1 22 4.699
4
c ELL008 Elliptocytosis-2 25 4.066
5
OVL001 Ovalocytosis, Southeast Asian 17 4.008
6
ALP035 Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis 23 3.386
7
ALP085 Alport Syndrome-Intellectual Disability-Midface Hypoplasia-Elliptocytosis Syndrome 20 2.383
8
PYR011 Pyropoikilocytosis 39 0.211
9
P HRD011 Hereditary Spherocytosis 52 0.181
10
P HML002 Hemolytic Anemia 52 0.128
11
P ALP004 Alport Syndrome 66 0.119
12
MLR004 Malaria 72 0.108
13
P THL005 Thalassemia 56 0.097
14
P ATX030 Ataxia-Telangiectasia 76 0.084
15
ART001 Arterial Tortuosity Syndrome 59 0.084
16
P HPT021 Hepatitis 58 0.084
17
P AND016 Andersen Syndrome 58 0.084
18
RNL007 Renal Tubular Acidosis 46 0.084
19
AND015 Androgen Insensitivity 65 0.069
20
P HRM001 Hermansky-Pudlak Syndrome 62 0.069
21
P AXN010 Axenfeld-Rieger Syndrome, Type 3 60 0.069
22
c PNC108 Pancreatitis, Hereditary 59 0.069
23
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.069
24
P TXP001 Toxoplasmosis 54 0.069
25
MLK003 Melkersson-Rosenthal Syndrome 53 0.069
26
PLS007 Plasmodium Falciparum Malaria 52 0.069
27
DFC004 Deficiency Anemia 52 0.069
28
HNT002 Hantavirus Pulmonary Syndrome 52 0.069
29
SNS001 Sensorineural Hearing Loss 49 0.069
30
c VRL010 Viral Hepatitis 49 0.069
31
P SHR029 Short Syndrome 49 0.069
32
THR013 Thoracic Outlet Syndrome 47 0.069
33
c HPT003 Hepatitis a 47 0.069
34
P STR020 Strabismus 47 0.069
35
PTN002 Patent Ductus Arteriosus 46 0.069
36
URB001 Urbach-Wiethe Disease 46 0.069
37
GLC085 Glucose-6-Phosphate Dehydrogenase Deficiency 46 0.069
38
P MYP006 Myopia 46 0.069
39
c CNG021 Congenital Toxoplasmosis 43 0.069
40
P TRC086 Trichohepatoenteric Syndrome 1 42 0.069
41
HMG005 Hemoglobinopathy 40 0.069
42
NRN002 Neuronitis 40 0.069
43
CHL004 Cholelithiasis 40 0.069
44
MNT002 Mental Depression 39 0.069
45
MNN014 Mononeuritis 39 0.069
46
VTM002 Vitamin B12 Deficiency 37 0.069
47
P INT063 Intellectual Disability 36 0.069
48
P HYP265 Hypotonia 35 0.069
49
HYP047 Hypertropia 31 0.069
50
PTN008 Patent Arterial Duct 29 0.069
51
c SPH013 Spherocytosis, Type 1 28 0.069
52
ALR002 Al-Raqad Syndrome 23 0.069
53
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 75 0.048
54
P OST002 Osteoporosis 75 0.048
55
ANR002 Aniridia 72 0.048
56
P PFF001 Pfeiffer Syndrome 71 0.048
57
P FML161 Familial Mediterranean Fever, Ar 67 0.048
58
c SPN225 Spondyloarthropathy 1 66 0.048
59
P ANG001 Angelman Syndrome 66 0.048
60
P RNL101 Renal Cell Carcinoma, Papillary 65 0.048
61
P PRM002 Primary Hyperoxaluria 64 0.048
62
KWS002 Kawasaki Disease 62 0.048
63
c CHR089 Chronic Kidney Failure 61 0.048
64
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.048
65
PGT001 Paget's Disease of Bone 57 0.048
66
c PRM005 Primary Hyperparathyroidism 56 0.048
67
IMG001 Image Syndrome 56 0.048
68
P RCK004 Rickets 55 0.048
69
KNS001 Kniest Dysplasia 55 0.048
70
P ACR001 Aicardi-Goutieres Syndrome 53 0.048
71
ACN002 Acanthosis Nigricans 53 0.048
72
P PRT010 Parathyroid Carcinoma 53 0.048
73
RPP001 Rapp-Hodgkin Syndrome 53 0.048
74
P HYP004 Hypercalcemia 52 0.048
75
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 52 0.048
76
P HYP069 Hyperparathyroidism 50 0.048
77
HYP609 Hypophosphatemic Rickets, X-Linked Dominant 49 0.048
78
P HYP098 Hypereosinophilic Syndrome 49 0.048
79
P GLM007 Glomerulonephritis 49 0.048
80
P NPH009 Nephrolithiasis 48 0.048
81
c SCN006 Secondary Syphilis 48 0.048
82
c PSD066 Pseudohypoparathyroidism, Type Ib 47 0.048
83
DGN001 Degenerative Disc Disease 47 0.048
84
LRN003 Learning Disability 47 0.048
85
MTP026 Metaphyseal Chondrodysplasia, Murk Jansen Type 46 0.048
86
c ART101 Aortic Valve Disease 2 46 0.048
87
STF001 Stiff-Person Syndrome 46 0.048
88
MYC002 Mycobacterium Avium Complex Disease 46 0.048
89
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.048
90
P HYP024 Hypoparathyroidism 45 0.048
91
MHR001 Mohr-Tranebjaerg Syndrome 45 0.048
92
P TMR015 Tumoral Calcinosis 44 0.048
93
URM002 Uremia 44 0.048
94
P GNT008 Giant Cell Tumor 43 0.048
95
IDP002 Idiopathic Juvenile Osteoporosis 43 0.048
96
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 43 0.048
97
OST011 Osteomalacia 42 0.048
98
P PSD015 Pseudohypoparathyroidism 42 0.048
99
MRC001 Marchiafava Bignami Disease 42 0.048
100
FBR009 Fibrous Dysplasia 42 0.048
101
CLC006 Calcinosis 42 0.048
102
OSS010 Ossification of the Posterior Longitudinal Ligament of the Spine 42 0.048
103
PGT008 Paget Disease of Bone 5, Juvenile-Onset 41 0.048
104
HYP063 Hypersplenism 40 0.048
105
P PRT029 Parathyroid Adenoma 39 0.048
106
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 39 0.048
107
HYP017 Hypophosphatemia 39 0.048
108
RNL011 Renal Osteodystrophy 39 0.048
109
ONC003 Oncogenic Osteomalacia 38 0.048
110
CLC001 Calciphylaxis 37 0.048
111
OST004 Osteitis Fibrosa 37 0.048
112
SML020 Small Patella Syndrome 37 0.048
113
HYP025 Hyperphosphatemia 36 0.048
114
GNT001 Giant Cell Reparative Granuloma 35 0.048
115
PRT030 Parathyroid Gland Disease 35 0.048
116
OST097 Osteoporotic Fracture 35 0.048
117
RTR008 Root Resorption 35 0.048
118
THL010 Thalassemia Minor 34 0.048
119
SPL018 Splenomegaly 34 0.048
120
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.048
121
PHS001 Phosphorus Metabolism Disease 33 0.048
122
GLC086 Glucocorticoid-Induced Osteoporosis 33 0.048
123
c GLL024 Gallbladder Disease 1 33 0.048
124
IDP073 Idiopathic Hypercalciuria 33 0.048
125
P HYP057 Hypervitaminosis D 32 0.048
126
SCN001 Secondary Hyperparathyroidism of Renal Origin 32 0.048
127
P ATX010 Ataxia Neuropathy Spectrum 31 0.048
128
NNT010 Nontoxic Goiter 31 0.048
129
AXL003 Axial Osteomalacia 30 0.048
130
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.048
131
c VTM007 Vitamin D-Dependent Rickets Type Ii 30 0.048
132
BLR008 Bilirubin Metabolic Disorder 30 0.048
133
BNG036 Bone Giant Cell Tumor 29 0.048
134
MNR003 Mineral Metabolism Disease 29 0.048
135
CLC007 Calcium Metabolism Disease 28 0.048
136
JNS003 Jensen Syndrome 28 0.048
137
BNR002 Bone Resorption Disease 28 0.048
138
BNR001 Bone Remodeling Disease 28 0.048
139
TFT003 Tufting Enteropathy 27 0.048
140
P RNL045 Renal Tubular Acidosis, Distal 26 0.048
141
IMP003 Impaired Renal Function Disease 23 0.048
142
GLC009 Glucosephosphate Dehydrogenase Deficiency 23 0.048
143
EXT012 Extraskeletal Chondroma 22 0.048
144
HYP268 Hypercalciuria, Absorptive 21 0.048
145
c BNG076 Benign Exophthalmos Syndrome 21 0.048
146
CHF001 Chief Cell Adenoma 20 0.048
147
SYN057 Syndromic Intellectual Disability 20 0.048
148
AND005 Androgen Insensitivity Syndrome, Mild 19 0.048
149
ANM026 Anemia, X-Linked, with/without Neutropenia and/or Platelet Abnormalities 16 0.048
150
c RHN011 Rh-Null Regulator Type Related Hemolytic Anemia 14 0.048
151
c SPT018 Sptb-Related Spherocytosis 11 0.048
152
c ANK011 Ank1-Related Spherocytosis 10 0.048