Search results for FDXR

56 hits were found for FDXR

# Family MCID Name MIFTS Score
1
ADT008 Auditory Neuropathy and Optic Atrophy 24 41.600
2
OPT078 Optic Atrophy-Ataxia-Peripheral Neuropathy-Global Developmental Delay Syndrome 15 22.149
3
P NRP001 Neuropathy 59 15.646
4
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 14.237
5
ATS010 Autosomal Recessive Disease 42 11.374
6
c 46X082 46,xy Sex Reversal 52 11.374
7
P FTL069 Fetal Akinesia Deformation Sequence 1 63 8.042
8
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 55 8.042
9
c HYP840 Hypercholesterolemia, Familial, 4 46 8.042
10
PGM029 Pigmentary Disorder, Reticulate, with Systemic Manifestations, X-Linked 49 8.042
11
c FML021 Familial Hypercholesterolemia 71 8.042
12
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 2.183
13
LNG019 Lung Combined Type Small Cell Carcinoma 32 2.183
14
P LNG021 Lung Occult Small Cell Carcinoma 20 2.183
15
P ADT009 Auditory Neuropathy Spectrum Disorder 33 2.115
16
HMS001 Hemosiderosis 48 2.003
17
P RRH023 Rare Hereditary Hemochromatosis 53 2.003
18
P MTC069 Mitochondrial Disorders 57 1.911
19
P PRP019 Peripheral Nervous System Disease 57 1.716
20
SNS003 Sensory Peripheral Neuropathy 51 1.537
21
MTC005 Mitochondrial Metabolism Disease 45 1.537
22
AGN016 Aging 54 1.486
23
RFC001 Rfc1 Canvas / Spectrum Disorder 5 1.248
24
P NRP066 Neuropathy, Hereditary Motor and Sensory, Type Via, with Optic Atrophy 42 1.176
25
LGH007 Leigh Syndrome 70 1.134
26
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.134
27
P MVM001 Movement Disease 61 1.134
28
P ENC018 Encephalopathy 62 1.134
29
XRD010 Xeroderma Pigmentosum, Variant Type 72 1.087
30
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 1.087
31
P BRS047 Breast Cancer 97 1.059
32
ACT228 Acute Radiation Syndrome 30 0.634
33
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.609
34
P MLN008 Melanoma 75 0.573
35
P PNC035 Pancreatic Cancer 86 0.573
36
SQM006 Squamous Cell Carcinoma 59 0.497
37
c NRB010 Neuroblastoma 1 60 0.471
38
P RTN008 Retinitis Pigmentosa 79 0.249
39
NRR001 Neuroretinitis 42 0.249
40
SVR004 Severe Combined Immunodeficiency 71 0.249
41
RTN023 Retinitis 45 0.249
42
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.176
43
P ATX030 Ataxia-Telangiectasia 80 0.176
44
P TST021 Testicular Germ Cell Tumor 61 0.176
45
HLX001 Helix Syndrome 47 0.176
46
c SML038 Small Cell Cancer of the Lung 69 0.176
47
XLN231 X-Linked Alport Syndrome 41 0.176
48
P ALP004 Alport Syndrome 70 0.176
49
TLN003 Telangiectasis 51 0.176
50
EMB004 Embryonal Carcinoma 55 0.176
51
GLM045 Glioma 62 0.176
52
ANX004 Anoxia 40 0.176
53
P NRB001 Neuroblastoma 66 0.176
54
GLL048 Glial Tumor 52 0.176
55
HYP266 Hypoxia 56 0.176
56
GRM010 Germ Cells Tumors 33 0.176
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