Search results for prx

56 hits were found for prx

# Family MCID Name MIFTS Score
1
CHR687 Charcot-Marie-Tooth Disease/hereditary Motor and Sensory Neuropathy 41 8.057
2
P CHR071 Charcot-Marie-Tooth Disease 65 6.872
3
c CHR670 Charcot-Marie-Tooth Disease, Demyelinating, Type 4f 43 6.738
4
P NRP063 Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive 57 6.562
5
HYP186 Hypertrophic Neuropathy of Dejerine-Sottas 51 4.744
6
P NRP001 Neuropathy 56 3.964
7
CHR629 Charcot-Marie-Tooth Disease and Deafness 52 3.429
8
TTH006 Tooth Disease 46 3.118
9
P PLY019 Polyneuropathy 56 3.048
10
SNS003 Sensory Peripheral Neuropathy 54 2.533
11
P SPN046 Spinal Muscular Atrophy 62 2.488
12
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 59 2.488
13
c HRD088 Hereditary Neuropathies 37 2.488
14
c SPN420 Spinocerebellar Ataxia 46 26 1.989
15
P PRP019 Peripheral Nervous System Disease 58 1.861
16
c CHR571 Charcot-Marie-Tooth Disease Type 5 17 1.861
17
c CHR521 Charcot-Marie-Tooth Disease, Type 4b1 46 1.817
19
NRM005 Neuromuscular Disease 64 1.760
20
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 1.760
21
P CHR625 Charcot-Marie-Tooth Disease, Demyelinating, Type 1b 57 1.760
22
P CHR640 Charcot-Marie-Tooth Disease, X-Linked Dominant, 1 56 1.760
23
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 55 1.760
24
c CHR420 Charcot-Marie-Tooth Disease, Type 4j 48 1.760
25
c CHR519 Charcot-Marie-Tooth Disease, Type 4b2 48 1.760
26
c CHR647 Charcot-Marie-Tooth Disease, Demyelinating, Type 1c 46 1.760
27
c CHR421 Charcot-Marie-Tooth Disease, Type 4h 46 1.760
28
c CHR517 Charcot-Marie-Tooth Disease, Type 4a 45 1.760
29
c CHR653 Charcot-Marie-Tooth Disease, Demyelinating, Type 1d 40 1.760
30
c CHR657 Charcot-Marie-Tooth Disease, Axonal, Type 2j 39 1.760
31
c CHR652 Charcot-Marie-Tooth Disease, Axonal, Type 2i 38 1.760
32
c CHR491 Charcot-Marie-Tooth Disease, Dominant Intermediate a 30 1.760
33
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 44 0.197
34
P DST101 Distal Hereditary Motor Neuropathies 32 0.197
35
P LNG064 Lung Cancer Susceptibility 3 78 0.098
36
TRM010 Traumatic Brain Injury 51 0.098
37
c HRD138 Hereditary Motor and Sensory Neuropathy V 32 0.098
38
P RRP027 Rare Peripheral Neuropathy 22 0.098
39
P LNG032 Lung Cancer 98 0.070
40
NRL016 Neural Tube Defects 82 0.070
41
P BLD134 Bladder Cancer 79 0.070
42
OST012 Osteoarthritis 78 0.070
43
P PRK057 Parkinson Disease, Late-Onset 78 0.070
44
FBR012 Fabry Disease 72 0.070
45
P TRN020 Turner Syndrome 67 0.070
46
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.070
47
P CTR002 Cataract 60 0.070
48
CRD132 Cardiac Conduction Defect 58 0.070
49
EMB004 Embryonal Carcinoma 56 0.070
50
47X002 47,xyy 49 0.070
51
BRN071 Brain Injury 49 0.070
52
P GND004 Gonadal Dysgenesis 48 0.070
53
HLX001 Helix Syndrome 47 0.070
54
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.070
55
BNG077 Benign Idiopathic Neonatal Seizures 26 0.070
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