Search results for nefl

74 hits were found for nefl

# Family MCID Name MIFTS Score
1
c CHR656 Charcot-Marie-Tooth Disease, Demyelinating, Type 1f 39 14.134
2
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 61 6.116
3
P CHR071 Charcot-Marie-Tooth Disease 64 4.988
4
c CHR676 Charcot-Marie-Tooth Disease, Dominant Intermediate G 25 4.361
5
TTH006 Tooth Disease 46 3.661
6
CHR629 Charcot-Marie-Tooth Disease and Deafness 54 3.390
7
P NRP001 Neuropathy 56 3.122
8
c AMY091 Amyotrophic Lateral Sclerosis 1 89 2.939
9
P ALZ034 Alzheimer Disease 88 2.871
10
P SCH015 Schizophrenia 75 2.871
11
P MLT020 Multiple Sclerosis 72 2.871
12
VSC002 Vascular Dementia 57 2.871
13
P PRP019 Peripheral Nervous System Disease 57 2.534
14
c CHR647 Charcot-Marie-Tooth Disease, Demyelinating, Type 1c 45 2.454
15
P AXN001 Axonal Neuropathy 36 2.454
16
P MTR014 Motor Neuron Disease 64 2.423
17
NRM005 Neuromuscular Disease 63 2.387
18
P PRK057 Parkinson Disease, Late-Onset 76 2.344
19
BRN028 Brain Cancer 73 2.344
20
P FRN006 Frontotemporal Dementia 70 2.344
21
P SPR120 Supranuclear Palsy, Progressive, 1 68 2.344
22
P SPN046 Spinal Muscular Atrophy 64 2.344
23
P NRP063 Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive 61 2.344
24
MTR007 Motor Peripheral Neuropathy 40 2.344
25
CHR687 Charcot-Marie-Tooth Disease/hereditary Motor and Sensory Neuropathy 40 2.220
26
P RRP027 Rare Peripheral Neuropathy 19 1.792
27
P OPT006 Optic Nerve Disease 57 1.713
28
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 56 1.713
29
HYP186 Hypertrophic Neuropathy of Dejerine-Sottas 51 1.713
30
PCK003 Pick Disease of Brain 68 1.658
31
DMN031 Dementia, Lewy Body 65 1.658
32
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 62 1.658
33
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 1.658
34
c EPL185 Epileptic Encephalopathy, Early Infantile, 39 47 1.658
35
c CHR646 Charcot-Marie-Tooth Disease, Axonal, Type 2b 47 1.658
36
P HRD094 Hereditary Motor and Sensory Neuropathy, Type Iic 45 1.658
37
c CHR352 Charcot-Marie-Tooth Disease, Axonal, Type 2f 44 1.658
38
P CMM008 Communicating Hydrocephalus 43 1.658
39
c CHR649 Charcot-Marie-Tooth Disease, Axonal, Type 2d 42 1.658
40
c CHR618 Charcot-Marie-Tooth Disease, Axonal, Type 2cc 41 1.658
41
c CHR657 Charcot-Marie-Tooth Disease, Axonal, Type 2j 41 1.658
42
P INT260 Intracranial Berry Aneurysm 40 1.658
43
c CHR353 Charcot-Marie-Tooth Disease, Axonal, Type 2l 39 1.658
44
c CHR651 Charcot-Marie-Tooth Disease, Axonal, Type 2b2 37 1.658
45
c ATM007 Autoimmune Disease of Central Nervous System 30 1.658
46
c CHR699 Charcot-Marie-Tooth Disease Type 2a2a 28 1.658
47
CHS002 Chiasmal Syndrome 26 1.658
48
P NRB001 Neuroblastoma 71 0.116
49
GLB015 Glioblastoma Multiforme 75 0.095
50
c BRN108 Branchiootic Syndrome 1 61 0.095
51
P LTR001 Lateral Sclerosis 53 0.095
52
P AST007 Astrocytoma 50 0.095
53
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.095
54
ACR006 Aceruloplasminemia 73 0.067
55
P MYP004 Myopathy 64 0.067
56
P GLM045 Glioma 63 0.067
57
c WLM018 Wilms Tumor 5 62 0.067
58
P SNS001 Sensorineural Hearing Loss 61 0.067
59
SQM006 Squamous Cell Carcinoma 60 0.067
60
P CHR640 Charcot-Marie-Tooth Disease, X-Linked Dominant, 1 56 0.067
61
P PLY019 Polyneuropathy 56 0.067
62
c MYP132 Myopathy, Congenital 55 0.067
63
SNS003 Sensory Peripheral Neuropathy 53 0.067
64
PTH003 Pathologic Nystagmus 51 0.067
65
P NML001 Nemaline Myopathy 51 0.067
66
GLL048 Glial Tumor 45 0.067
67
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 45 0.067
68
P HYP265 Hypotonia 42 0.067
70
c HRD088 Hereditary Neuropathies 37 0.067
71
P HRD217 Hereditary Optic Neuropathy 34 0.067
72
P DST101 Distal Hereditary Motor Neuropathies 32 0.067
73
P ATS426 Autosomal Dominant Distal Hereditary Motor Neuronopathy 26 0.067
74
CRB212 Cerebellar Ataxia with Peripheral Neuropathy 8 0.067
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