Search results for plp1

120 hits were found for plp1

# Family MCID Name MIFTS Score
1
P PLZ001 Pelizaeus-Merzbacher Disease 64 13.852
2
PLP007 Plp1 Disorders 9 7.425
3
P SPS133 Spastic Paraplegia 2, X-Linked 49 5.222
4
PRP016 Paraplegia 52 4.160
5
P LKD001 Leukodystrophy 59 3.713
6
c HRD010 Hereditary Spastic Paraplegia 66 3.174
7
P SCH015 Schizophrenia 74 2.767
8
SPS004 Spastic Quadriplegia 39 2.767
9
P MLT020 Multiple Sclerosis 72 2.715
10
CRB037 Cerebral Palsy 69 2.715
11
c PRM108 Primary Progressive Multiple Sclerosis 51 2.715
12
P MYS003 Myasthenia Gravis 68 2.683
13
P CHR071 Charcot-Marie-Tooth Disease 65 2.683
14
ATM095 Autoimmune Disease 62 2.683
15
P OPT009 Optic Neuritis 57 2.683
16
DMY004 Demyelinating Disease 52 2.683
17
QDR001 Quadriplegia 48 2.287
18
P DYS154 Dystonia 65 2.228
19
RLP002 Relapsing-Remitting Multiple Sclerosis 56 2.228
20
c CNT035 Central Nervous System Disease 52 2.228
21
P MTC003 Metachromatic Leukodystrophy 70 2.191
22
P OLG002 Oligodendroglioma 67 2.191
23
P NRN021 Neuronal Ceroid Lipofuscinosis 64 2.191
24
P NMN002 Niemann-Pick Disease 59 2.191
25
P SBS003 Substance Abuse 55 2.191
26
CHR629 Charcot-Marie-Tooth Disease and Deafness 52 2.191
27
c MGL009 Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 50 2.191
28
CCN002 Cocaine Abuse 49 2.191
29
P HYP700 Hypomyelinating Leukodystrophy 33 1.742
30
PLZ007 Pelizaeus-Merzbacher Disease, Classic Form 11 1.694
31
LBS001 Lubs X-Linked Mental Retardation Syndrome 51 1.635
32
PLZ008 Pelizaeus-Merzbacher Disease, Transitional Form 9 1.635
33
c PLZ002 Pelizaeus-Merzbacher-Like Disease 36 1.598
34
PLZ009 Pelizaeus-Merzbacher Disease in Female Carriers 5 1.598
35
ARN001 Arena Syndrome 5 1.598
36
P KRB001 Krabbe Disease 69 1.549
37
c NMN013 Niemann-Pick Disease, Type a 62 1.549
38
CNV004 Canavan Disease 61 1.549
39
LKN001 Leukoencephalopathy with Vanishing White Matter 59 1.549
40
ALX003 Alexander Disease 59 1.549
41
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 1.549
42
ALL001 Allan-Herndon-Dudley Syndrome 56 1.549
43
c LKD010 Leukodystrophy, Hypomyelinating, 2 49 1.549
44
LKD025 Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant 48 1.549
45
c LKD009 Leukodystrophy, Hypomyelinating, 5 46 1.549
46
SPS007 Spastic Cerebral Palsy 45 1.549
47
BNS003 Binswanger's Disease 42 1.549
48
CRB033 Cerebral Degeneration 42 1.549
49
P MGL010 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a 40 1.549
50
c SPS213 Spastic Paraplegia 75, Autosomal Recessive 39 1.549
51
c LKD018 Leukodystrophy, Hypomyelinating, 8, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 38 1.549
52
ALL014 Allergic Encephalomyelitis 38 1.549
53
c SPS096 Spastic Paraplegia 44, Autosomal Recessive 37 1.549
54
c HRD088 Hereditary Neuropathies 37 1.549
55
c CRD114 Cardiomyopathy, Dilated, 1m 36 1.549
56
c LKD008 Leukodystrophy, Hypomyelinating, 4 34 1.549
57
XLN228 X-Linked Recessive Disease 26 1.549
58
P PRH002 Pure Hereditary Spastic Paraplegia 22 1.549
59
c SPS229 Spastic Ataxia 8 19 1.549
60
c XLN230 X-Linked Monogenic Disease 18 1.549
61
HYP659 Hypomyelinating Leukoencephalopathy 18 1.549
62
XLN237 X-Linked Pure Spastic Paraplegia 8 1.549
63
PTH003 Pathologic Nystagmus 52 0.194
64
SPS057 Spasticity 45 0.185
65
P NRP001 Neuropathy 56 0.143
66
P PRP019 Peripheral Nervous System Disease 58 0.131
67
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.117
68
SPS019 Spastic Paraparesis 38 0.117
69
P PRS049 Persistent Mullerian Duct Syndrome 50 0.083
70
DYS073 Dysphagia 50 0.083
71
P HYP265 Hypotonia 43 0.083
72
P AXN001 Axonal Neuropathy 36 0.083
73
P ATX030 Ataxia-Telangiectasia 82 0.059
74
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.059
75
ULC004 Ulcerative Colitis 73 0.059
76
P ATS364 Autism 70 0.059
77
P OCL013 Oculodentodigital Dysplasia 69 0.059
78
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.059
79
c PRM196 Premature Ovarian Failure 1 67 0.059
80
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.059
81
ART001 Arterial Tortuosity Syndrome 66 0.059
82
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.059
83
CLR108 Colorectal Adenoma 64 0.059
84
P ANR048 Aniridia 1 63 0.059
85
ANR007 Anorexia Nervosa 63 0.059
86
CLT003 Colitis 62 0.059
87
P TRC086 Trichohepatoenteric Syndrome 1 62 0.059
88
P SCL018 Scoliosis 60 0.059
89
ACN002 Acanthosis Nigricans 60 0.059
90
P MCR010 Microcephaly 59 0.059
91
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.059
92
IRN002 Iron Metabolism Disease 57 0.059
93
c MCR256 Microphthalmia, Syndromic 9 56 0.059
94
P PLY019 Polyneuropathy 56 0.059
95
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.059
96
P ALP106 Alport Syndrome 1, X-Linked 55 0.059
97
THR013 Thoracic Outlet Syndrome 54 0.059
98
OPT054 Opitz-Kaveggia Syndrome 54 0.059
99
P TRM003 Tremor 54 0.059
100
SPS003 Spastic Diplegia 51 0.059
101
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.059
102
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.059
103
SPN028 Spondyloepimetaphyseal Dysplasia, Strudwick Type 49 0.059
104
P DMY001 Demyelinating Polyneuropathy 43 0.059
105
c PRS128 Persistent Mullerian Duct Syndrome, Types I and Ii 42 0.059
106
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.059
107
c LKD015 Leukodystrophy, Hypomyelinating, 3 40 0.059
108
HTR014 Heterotaxy, Visceral, 1, X-Linked 40 0.059
109
CRB009 Cerebritis 37 0.059
110
ATX010 Ataxia Neuropathy Spectrum 34 0.059
111
SPN438 Spondyloepimetaphyseal Dysplasia, X-Linked, with Hypomyelinating Leukodystrophy 34 0.059
112
ACT064 Acute Necrotizing Encephalitis 33 0.059
113
TRG019 Trigonocephaly with Short Stature and Developmental Delay 32 0.059
114
ISL119 Isolated Optic Neuritis 30 0.059
115
MYC088 Mycobacterium Avium Complex Infections 29 0.059
116
CMP097 Complex Chromosomal Rearrangement 25 0.059
117
AND005 Androgen Insensitivity Syndrome, Mild 19 0.059
118
c MLT031 Multiple Epiphyseal Dysplasia, Recessive 19 0.059
119
BLD137 Blood Group--Ahonen 16 0.059
120
FGS006 Fg Syndrome 5 11 0.059
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