78 hits were found for 'PMP22'

# ++ Fam MCID Name MIFTS Score
1
P CHR071 Charcot-Marie-Tooth Disease 61 5.844
2
c CHR129 Charcot-Marie-Tooth Disease Type 1a 41 5.055
3
P HRD025 Hereditary Neuropathy with Liability to Pressure Palsies 23 4.363
4
NRP016 Neuropathy, Recurrent, with Pressure Palsies 21 4.363
5
NRP001 Neuropathy 54 4.128
6
TTH006 Tooth Disease 54 4.052
7
c CHR133 Charcot-Marie-Tooth Disease Type 1e 23 3.847
8
c HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 19 3.587
9
HRD088 Hereditary Neuropathies 35 3.562
10
c CHR113 Charcot-Marie-Tooth Neuropathy Type 1 25 3.562
11
c CHR289 Charcot-Marie-Tooth Neuropathy Type 1a 12 3.562
12
c CNG102 Congenital Hypomyelination Neuropathy 23 2.965
13
PLY020 Polyradiculoneuropathy 45 2.938
14
P PLZ001 Pelizaeus-Merzbacher Disease 66 2.908
15
DBT010 Diabetic Neuropathy 59 2.908
16
ACT049 Acute Disseminated Encephalomyelitis 56 2.908
17
P PLY019 Polyneuropathy 54 2.908
18
GLL022 Guillain-Barre Syndrome 54 2.908
19
GLL031 Guillain-Barr´┐Ż Syndrome 54 2.908
20
P CRP001 Carpal Tunnel Syndrome 53 2.908
21
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 48 2.908
22
NRN002 Neuronitis 47 2.908
23
HRD026 Hereditary Ataxia 45 2.908
24
ASC002 Ascariasis 44 2.908
25
HRD030 Hereditary Neuralgic Amyotrophy 42 2.908
26
c CHR022 Charcot-Marie-Tooth Disease Type 1 40 2.908
27
KRT049 Keratosis Follicularis 35 2.908
28
MNN017 Mononeuropathy 35 2.908
29
FTD001 Foot Drop 30 2.908
30
c CHR130 Charcot-Marie-Tooth Disease Type 1b 29 2.908
31
BRC010 Brachial Plexus Lesion 28 2.908
32
KRT014 Keratosis Follicularis Spinulosa Decalvans 24 2.908
33
SNS009 Sensory Neuropathy Type 1 20 2.908
34
INH006 Inherited Peripheral Neuropathy 15 2.908
35
PRP023 Peripheral Neuropathy 46 2.657
36
P OST018 Osteosarcoma 70 2.582
37
P MLT020 Multiple Sclerosis 75 2.519
38
c DBT009 Diabetes Mellitus 68 2.519
39
NRT004 Neuritis 46 2.519
40
c CHR293 Charcot-Marie-Tooth Neuropathy Type 1e 6 2.519
41
AXN001 Axonal Neuropathy 44 2.131
42
P BRS047 Breast Cancer 85 2.097
43
SNS001 Sensorineural Hearing Loss 55 2.097
44
SRC014 Sarcoma 54 2.097
45
P AMY001 Amyotrophic Lateral Sclerosis 87 2.057
46
c PNC044 Pancreatitis 58 2.057
47
SLP006 Sleep Apnea 57 2.057
48
c ATX004 Ataxia 56 2.057
49
c BLN003 Blindness 54 2.057
50
c LTR001 Lateral Sclerosis 52 2.057
51
c MYP004 Myopathy 52 2.057
52
KRT009 Keratosis 49 2.057
53
c MYT002 Myotonic Dystrophy 49 2.057
54
ENC006 Encephalomyelitis 49 2.057
55
P NRM005 Neuromuscular Disease 48 2.057
56
c DMY001 Demyelinating Polyneuropathy 45 2.057
57
TRC012 Trichuriasis 42 2.057
58
NRL007 Neurologic Diseases 41 2.057
59
c CHR024 Charcot-Marie-Tooth Disease Type 3 33 2.057
60
BRC011 Brachial Plexus Neuropathy 31 2.057
61
NRP034 Neuropathy, Inflammatory Demyelinating 23 2.057
62
WSR001 Was-Related Disorders 22 2.057
63
P MLT019 Multiple Myeloma 76 1.454
64
c MYL007 Myeloma 53 1.454
65
P KRT007 Keratoconus 46 1.454
66
CRB009 Cerebritis 46 1.454
67
CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 20 0.126
68
P RSP003 Respiratory Failure 60 0.063
69
P HRD021 Hereditary Sensory Neuropathy 49 0.063
70
BRS051 Breast Disease 48 0.063
71
c LFT003 Left Ventricular Noncompaction 48 0.063
72
P ATS008 Autosomal Dominant Disease 45 0.063
73
CHR101 Char Syndrome 42 0.063
74
WLL004 Wallerian Degeneration 41 0.063
75
c ATS010 Autosomal Recessive Disease 39 0.063
76
c FML056 Familial Deafness 24 0.063
77
FCL011 Facial Nerve Disease 12 0.063
78
HYP186 Hypertrophic Neuropathy of Dejerine-Sottas 10 0.063