Search results for SLC29A3

94 hits were found for SLC29A3

# Family MCID Name MIFTS Score
1
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 56 85.698
2
ASR001 Asrar Facharzt Haque Syndrome 14 81.175
3
P HYP077 Hypertrichosis 48 20.079
4
HST010 Histiocytosis 49 19.626
5
DYS045 Dysosteosclerosis 36 18.643
6
P DBT009 Diabetes Mellitus 67 17.488
7
P SNS001 Sensorineural Hearing Loss 60 15.527
8
P OST001 Osteopetrosis 70 12.678
9
RHN002 Rhinoscleroma 36 12.301
10
PLY010 Polyclonal Hypergammaglobulinemia 35 11.265
11
RSD004 Rosai-Dorfman Disease 49 10.792
12
P HRD018 Hair Disease 43 7.965
13
c DWL002 Dowling-Degos Disease 1 58 3.098
14
HYP080 Hypogonadism 49 2.568
15
ATS010 Autosomal Recessive Disease 42 2.108
16
ERY069 Erythrokeratoderma ''en Cocardes'' 26 2.018
17
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.908
18
c BRN108 Branchiootic Syndrome 1 63 1.466
19
BNN005 Bunion 32 1.413
20
EXC002 Exocrine Pancreatic Insufficiency 42 1.240
21
P RCT021 Rectum Cancer 54 1.157
22
HYP066 Hyperglycemia 60 1.070
23
HMP001 Hemopericardium 47 1.037
24
P PRC012 Pericardial Effusion 50 1.037
25
P UVT001 Uveitis 57 1.037
26
CNG506 Congenital Amyoplasia 27 1.037
27
c SML038 Small Cell Cancer of the Lung 68 0.999
28
P HYP730 Hypogonadotropic Hypogonadism 57 0.999
29
ATN021 Autoinflammatory Syndrome 30 0.999
30
MCK007 Muckle-Wells Syndrome 64 0.957
31
WLL006 Wells Syndrome 49 0.957
32
EXP004 Exophthalmos 50 0.957
33
P LNG021 Lung Occult Small Cell Carcinoma 20 0.941
34
LNG019 Lung Combined Type Small Cell Carcinoma 34 0.941
35
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.941
36
HYP001 Hypochromic Microcytic Anemia 36 0.907
37
PYC001 Pycnodysostosis 55 0.907
38
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 36 0.907
39
PCT003 Pectus Excavatum 43 0.907
40
LYS002 Lysosomal Storage Disease 51 0.907
42
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.841
43
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.841
44
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.841
45
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.841
46
IMM167 Immune Deficiency Disease 76 0.841
47
CMB007 Combined Immunodeficiency 56 0.841
48
LYM027 Lymphopenia 56 0.841
49
P PRR002 Pure Red-Cell Aplasia 46 0.841
50
P ART023 Arthropathy 59 0.841
51
HYD002 Hydronephrosis 58 0.841
52
SKN016 Skin Disease 63 0.841
53
c LCL006 Localized Scleroderma 64 0.841
54
RTR011 Retroperitoneal Fibrosis 47 0.841
55
IMM023 Immunodeficiency Without Anhidrotic Ectodermal Dysplasia 16 0.841
56
SCL025 Scleromyxedema 37 0.841
57
RYN005 Raynaud Phenomenon 45 0.841
58
CTN020 Cutaneous Sclerosis 16 0.841
59
P PNC035 Pancreatic Cancer 87 0.797
60
P BRS047 Breast Cancer 97 0.573
61
CLL010 Cellular Ependymoma 58 0.573
62
c OST136 Osteopetrosis, Autosomal Recessive 7 50 0.316
63
c TYP008 Type 1 Diabetes Mellitus 77 0.274
64
P BND020 Bone Disease 60 0.274
65
P HYP750 Hypertriglyceridemia, Familial 61 0.223
66
PRP016 Paraplegia 52 0.223
67
MNT002 Mental Depression 56 0.223
68
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.223
69
SPS019 Spastic Paraparesis 38 0.223
70
PRT251 Proteinuria, Chronic Benign 58 0.158
71
CYS001 Cystic Fibrosis 77 0.158
72
P FML018 Familial Mediterranean Fever 73 0.158
73
c PGT009 Paget Disease of Bone 2, Early-Onset 34 0.158
74
MJD001 Majeed Syndrome 39 0.158
75
P EPL074 Epilepsy, Hot Water, 1 17 0.158
76
FML345 Familial Expansile Osteolysis 46 0.158
77
P LPR021 Leprosy 3 71 0.158
78
P MMB011 Membranous Nephropathy 50 0.158
79
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.158
80
c ATR087 Atrial Standstill 1 74 0.158
81
MNR012 Meniere Disease 55 0.158
82
c WLF013 Wolfram Syndrome 1 60 0.158
83
MVL001 Mevalonic Aciduria 65 0.158
84
STN011 Sting-Associated Vasculopathy with Onset in Infancy 44 0.158
85
c ATM011 Autoimmune Hepatitis 62 0.158
86
RFL002 Reflex Epilepsy 40 0.158
87
P PGT001 Paget's Disease of Bone 60 0.158
88
BRC012 Brucellosis 66 0.158
89
P SYS005 Systemic Scleroderma 73 0.158
90
AZS001 Azoospermia 45 0.158
91
P INF032 Infertility 60 0.158
92
HNS001 Hansen's Disease 32 0.158
93
PRM334 Primary Bone Dysplasia with Increased Bone Density 15 0.158
94
MNG006 Monogenic Diabetes 45 0.158
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