73 hits were found for 'PMP22'

# Family MCID Name MIFTS Score
1
c CHR071 Charcot-Marie-Tooth Disease 69 5.876
2
c CHR129 Charcot-Marie-Tooth Disease Type 1a 51 5.079
3
HRD025 Hereditary Neuropathy with Liability to Pressure Palsies 36 4.677
4
NRP016 Neuropathy, Recurrent, with Pressure Palsies 29 4.383
5
NRP001 Neuropathy 61 4.218
6
TTH006 Tooth Disease 55 4.077
7
c CHR133 Charcot-Marie-Tooth Disease Type 1e 32 3.865
8
c CHR113 Charcot-Marie-Tooth Neuropathy Type 1 29 3.627
9
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 21 3.604
10
HRD088 Hereditary Neuropathies 31 3.578
11
c CHR289 Charcot-Marie-Tooth Neuropathy Type 1a 16 3.578
12
c CHR022 Charcot-Marie-Tooth Disease Type 1 45 2.980
13
NRN002 Neuronitis 64 2.952
14
PLY020 Polyradiculoneuropathy 52 2.952
15
P PLZ001 Pelizaeus-Merzbacher Disease 78 2.922
16
DBT010 Diabetic Neuropathy 68 2.922
17
P PLY019 Polyneuropathy 64 2.922
18
GLL022 Guillain-Barre Syndrome 63 2.922
19
ACT049 Acute Disseminated Encephalomyelitis 60 2.922
20
P CRP001 Carpal Tunnel Syndrome 55 2.922
21
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 51 2.922
22
HRD030 Hereditary Neuralgic Amyotrophy 51 2.922
23
HRD026 Hereditary Ataxia 48 2.922
24
ASC002 Ascariasis 47 2.922
25
MNN017 Mononeuropathy 43 2.922
26
c CHR130 Charcot-Marie-Tooth Disease Type 1b 41 2.922
27
KRT049 Keratosis Follicularis 37 2.922
28
BRC010 Brachial Plexus Lesion 28 2.922
29
SNS009 Sensory Neuropathy Type 1 23 2.922
30
FTD001 Foot Drop 21 2.922
31
KRT014 Keratosis Follicularis Spinulosa Decalvans 21 2.922
32
CNG102 Congenital Hypomyelination Neuropathy 20 2.922
33
INH006 Inherited Peripheral Neuropathy 17 2.922
34
PRP023 Peripheral Neuropathy 53 2.771
35
P OST018 Osteosarcoma 81 2.595
36
P MLT020 Multiple Sclerosis 82 2.530
37
c DBT009 Diabetes Mellitus 80 2.530
38
NRT004 Neuritis 51 2.530
39
c CHR293 Charcot-Marie-Tooth Neuropathy Type 1e 10 2.530
40
AXN001 Axonal Neuropathy 45 2.141
41
P BRS047 Breast Cancer 105 2.107
42
SRC014 Sarcoma 63 2.107
43
SNS001 Sensorineural Hearing Loss 56 2.107
44
P AMY001 Amyotrophic Lateral Sclerosis 100 2.066
45
c PNC044 Pancreatitis 67 2.066
46
P MYP004 Myopathy 58 2.066
47
c LTR001 Lateral Sclerosis 55 2.066
48
NRM005 Neuromuscular Disease 55 2.066
49
ENC006 Encephalomyelitis 55 2.066
50
c MYT002 Myotonic Dystrophy 54 2.066
51
KRT009 Keratosis 53 2.066
52
c DMY001 Demyelinating Polyneuropathy 53 2.066
53
P CHR024 Charcot-Marie-Tooth Disease Type 3 45 2.066
54
c SLP006 Sleep Apnea 44 2.066
55
NRL007 Neurologic Diseases 44 2.066
56
TRC012 Trichuriasis 43 2.066
57
c ATX004 Ataxia 38 2.066
58
c BLN003 Blindness 37 2.066
59
BRC011 Brachial Plexus Neuropathy 33 2.066
60
WSR001 Was-Related Disorders 28 2.066
61
NRP034 Neuropathy, Inflammatory Demyelinating 21 2.066
62
P MLT019 Multiple Myeloma 89 1.461
63
c MYL007 Myeloma 59 1.461
64
CRB009 Cerebritis 56 1.461
65
c KRT007 Keratoconus 50 1.461
66
CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 23 0.129
67
P RSP003 Respiratory Failure 70 0.064
68
P HRD021 Hereditary Sensory Neuropathy 58 0.064
69
BRS051 Breast Disease 56 0.064
70
P ATS008 Autosomal Dominant Disease 46 0.064
71
c ATS010 Autosomal Recessive Disease 39 0.064
72
FCL011 Facial Nerve Disease 17 0.064
73
HYP186 Hypertrophic Neuropathy of Dejerine-Sottas 11 0.064