Search results for elliptocytosis

74 hits were found for elliptocytosis

# Family MCID Name MIFTS Score
1
P HRD012 Hereditary Elliptocytosis 41 8.494
2
OVL001 Ovalocytosis, Southeast Asian 30 7.184
3
c ELL005 Elliptocytosis 2 29 6.146
4
c ELL010 Elliptocytosis 1 22 6.131
5
AMM001 Amme Complex 16 4.039
6
MDF002 Midface Hypoplasia, Hearing Impairment, Elliptocytosis, and Nephrocalcinosis 16 3.382
7
ALP085 Alport Syndrome-Intellectual Disability-Midface Hypoplasia-Elliptocytosis Syndrome 21 3.339
8
RDC013 Red Cell Permeability Defect 8 2.344
9
PYR040 Pyropoikilocytosis, Hereditary 35 0.236
10
P HRD011 Hereditary Spherocytosis 55 0.228
11
P HML002 Hemolytic Anemia 62 0.172
12
MLR004 Malaria 86 0.149
13
P THL005 Thalassemia 65 0.149
14
ALP046 Alport Syndrome, X-Linked 74 0.136
15
P ANR048 Aniridia 1 68 0.122
16
P RNL007 Renal Tubular Acidosis 51 0.122
17
ANR038 Anorexia Nervosa 1 21 0.122
18
BLD137 Blood Group--Ahonen 17 0.122
19
HYD063 Hydroxyacyl Glutathione Hydrolase Deficiency 11 0.122
20
P HPT021 Hepatitis 75 0.106
21
c BTT014 Beta-Thalassemia 70 0.106
22
AGN016 Aging 65 0.106
23
c BLD140 Blood Group, I System 37 0.106
24
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.106
25
P FML018 Familial Mediterranean Fever 73 0.086
26
P TXP001 Toxoplasmosis 65 0.086
27
c HPT003 Hepatitis a 63 0.086
28
THR024 Thrombosis 61 0.086
29
c VRL010 Viral Hepatitis 59 0.086
30
PLS007 Plasmodium Falciparum Malaria 59 0.086
31
c CNG021 Congenital Toxoplasmosis 57 0.086
32
P HMG032 Hemoglobin H Disease 53 0.086
33
HMG005 Hemoglobinopathy 53 0.086
34
CHL004 Cholelithiasis 51 0.086
35
HYP063 Hypersplenism 49 0.086
36
VTM002 Vitamin B12 Deficiency 46 0.086
37
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 46 0.086
38
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.086
39
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.086
40
BLD164 Blood Group, Gerbich System 18 0.086
41
HML050 Hemolytic Poikilocytic Anemia Due to Reduced Ankyrin Binding Sites 8 0.086
42
P LKM002 Leukemia 75 0.061
43
BRC012 Brucellosis 71 0.061
44
P MYL006 Myeloid Leukemia 69 0.061
45
DFC004 Deficiency Anemia 62 0.061
46
ATH013 Atherosclerosis Susceptibility 59 0.061
47
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 59 0.061
48
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 59 0.061
49
PLS006 Plasmodium Vivax Malaria 56 0.061
50
THR004 Thrombocytosis 55 0.061
51
ART001 Arterial Tortuosity Syndrome 53 0.061
52
c SPH013 Spherocytosis, Type 1 53 0.061
53
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.061
54
RTN023 Retinitis 52 0.061
55
RPP001 Rapp-Hodgkin Syndrome 51 0.061
56
NPH003 Nephrocalcinosis 49 0.061
57
GLC009 Glucosephosphate Dehydrogenase Deficiency 48 0.061
58
RFR010 Refractory Anemia 48 0.061
59
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 48 0.061
60
HYP458 Hyper Ige Syndrome 46 0.061
61
SPL018 Splenomegaly 45 0.061
62
MLK003 Melkersson-Rosenthal Syndrome 42 0.061
63
P RNL045 Renal Tubular Acidosis, Distal 42 0.061
64
c CNG208 Congenital Disorder of Glycosylation, Type Iic 42 0.061
65
CRB009 Cerebritis 41 0.061
66
NNT011 Neonatal Anemia 35 0.061
67
c RNL047 Renal Tubular Acidosis, Distal, Autosomal Recessive 35 0.061
68
P RFR008 Refractory Anemia with Excess Blasts 34 0.061
69
VGN019 Vaginal Discharge 34 0.061
70
ALR002 Al-Raqad Syndrome 30 0.061
71
CRY019 Cryohydrocytosis 29 0.061
72
SYN057 Syndromic Intellectual Disability 27 0.061
73
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 20 0.061
74
OVL006 Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis 8 0.061
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