|
#
|
Concept name
|
Type
|
Relation
|
Support
|
Score
|
|
1
|
smooth muscle atrophy
|
Disease
|
Known
|
Explain
|
162.15228
|
|
2
|
smooth muscle hyperplasia
|
Function
|
Known
|
Explain
|
151.93145
|
|
3
|
smooth muscle hypertrophy
|
Disease
|
Known
|
Explain
|
130.31583
|
|
4
|
muscle adaptation
|
Function
|
Known
|
Explain
|
108.73264
|
|
5
|
Muscular Atrophy
|
Disease
|
Inferred
|
Explain
|
26.33969
|
|
6
|
Muscle hypertrophy
|
Function
|
Inferred
|
Explain
|
4.61662
|
|
7
|
IL1B gene
|
Gene
|
Known
|
Explain
|
4.05013
|
|
8
|
striated muscle adaptation
|
Function
|
Inferred
|
Explain
|
2.89897
|
|
9
|
muscle hypertrophy in response to stress
|
Function
|
Inferred
|
Explain
|
2.51409
|
|
10
|
muscle system process
|
Function
|
Inferred
|
Explain
|
2.08432
|
|
11
|
striated muscle atrophy
|
Disease
|
Inferred
|
Explain
|
1.44893
|
|
12
|
NOS3 gene
|
Gene
|
Inferred
|
Explain
|
1.13358
|
|
13
|
HMOX1 gene
|
Gene
|
Inferred
|
Explain
|
1.11309
|
|
14
|
CYBA gene
|
Gene
|
Inferred
|
Explain
|
0.73322
|
|
15
|
cardiac muscle adaptation
|
Function
|
Inferred
|
Explain
|
0.54663
|
|
16
|
Amyotrophy, monomelic
|
Disease
|
Inferred
|
Explain
|
0.49612
|
|
17
|
skeletal muscle adaptation
|
Function
|
Inferred
|
Explain
|
0.47218
|
|
18
|
Muscular Atrophy, Spinal, Type II
|
Disease
|
Inferred
|
Explain
|
0.43882
|
|
19
|
Scapuloperoneal Form of Spinal Muscular Atrophy
|
Disease
|
Inferred
|
Explain
|
0.43290
|
|
20
|
Primrose syndrome
|
Disease
|
Inferred
|
Explain
|
0.40226
|
|
21
|
Juvenile Spinal Muscular Atrophy
|
Disease
|
Inferred
|
Explain
|
0.39235
|
|
22
|
HMN (Hereditary Motor Neuropathy) Proximal Type I
|
Disease
|
Inferred
|
Explain
|
0.37629
|
|
23
|
AMYOTROPHY, HEREDITARY NEURALGIC
|
Disease
|
Inferred
|
Explain
|
0.36624
|
|
24
|
cardiac muscle atrophy
|
Disease
|
Inferred
|
Explain
|
0.34482
|
|
25
|
Atrophic
|
Disease
|
Inferred
|
Explain
|
0.31723
|
|
26
|
Hyperkalemic periodic paralysis
|
Disease
|
Inferred
|
Explain
|
0.30385
|
|
27
|
Spinal Muscular Atrophy
|
Disease
|
Inferred
|
Explain
|
0.30137
|
|
28
|
MUSCULAR ATROPHY, ATAXIA, RETINITIS PIGMENTOSA, AND DIABETES MELLITUS
|
Other
|
Inferred
|
Explain
|
0.30120
|
|
29
|
Allan-Herndon-Dudley syndrome (AHDS)
|
Disease
|
Inferred
|
Explain
|
0.29839
|
|
30
|
Carpal Tunnel Syndrome
|
Disease
|
Inferred
|
Explain
|
0.28974
|
|
31
|
Wieacker-Wolff syndrome
|
Disease
|
Inferred
|
Explain
|
0.28683
|
|
32
|
cardiac muscle hypertrophy in response to stress
|
Function
|
Inferred
|
Explain
|
0.26024
|
|
33
|
MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, SMALL TESTES, MUSCLE WASTING, AND TREMOR
|
Disease
|
Inferred
|
Explain
|
0.25913
|
|
34
|
Neuromuscular Manifestations
|
Disease
|
Inferred
|
Explain
|
0.24535
|
|
35
|
skeletal muscle atrophy
|
Function
|
Inferred
|
Explain
|
0.19949
|
|
36
|
striated muscle hypertrophy
|
Function
|
Inferred
|
Explain
|
0.19176
|
|
37
|
Russell-Silver syndrome
|
Disease
|
Inferred
|
Explain
|
0.16093
|
|
38
|
AMPD1 gene
|
Gene
|
Inferred
|
Explain
|
0.11592
|
|
39
|
TBCE gene
|
Gene
|
Inferred
|
Explain
|
0.10604
|
|
40
|
TRIM72 gene
|
Gene
|
Inferred
|
Explain
|
0.09134
|
|
41
|
skeletal muscle hypertrophy
|
Disease
|
Inferred
|
Explain
|
0.08822
|
|
42
|
Nonprogressive
|
Disease
|
Inferred
|
Explain
|
0.08600
|
|
43
|
Muscle relaxation phase
|
Function
|
Inferred
|
Explain
|
0.08315
|
|
44
|
system process
|
Function
|
Inferred
|
Explain
|
0.07506
|
|
45
|
Mental deficiency
|
Disease
|
Inferred
|
Explain
|
0.06745
|
|
46
|
Brachial Plexus Neuropathies
|
Disease
|
Inferred
|
Explain
|
0.05944
|
|
47
|
SMN1 gene
|
Gene
|
Inferred
|
Explain
|
0.05594
|
|
48
|
Neuritis
|
Disease
|
Inferred
|
Explain
|
0.05213
|
|
49
|
SPINAL MUSCULAR ATROPHY, CHILDHOOD, PROXIMAL, AUTOSOMAL DOMINANT
|
Disease
|
Inferred
|
Explain
|
0.04908
|
|
50
|
Myokymia
|
Disease
|
Inferred
|
Explain
|
0.04401
|
|
51
|
skeletal muscle fiber adaptation
|
Function
|
Inferred
|
Explain
|
0.04370
|
|
52
|
SMN2 gene
|
Gene
|
Inferred
|
Explain
|
0.03940
|
|
53
|
Muscle hypotonia
|
Disease
|
Inferred
|
Explain
|
0.03528
|
|
54
|
KCNH2 gene
|
Gene
|
Inferred
|
Explain
|
0.03492
|
|
55
|
Myotonia
|
Disease
|
Inferred
|
Explain
|
0.03456
|
|
56
|
cardiac muscle hypertrophy
|
Function
|
Inferred
|
Explain
|
0.03363
|
|
57
|
Median Neuropathy
|
Disease
|
Inferred
|
Explain
|
0.03055
|
|
58
|
Pontocerebellar Hypoplasia Type 1
|
Disease
|
Inferred
|
Explain
|
0.02863
|
|
59
|
Congenital contractures
|
Other
|
Inferred
|
Explain
|
0.02837
|
|
60
|
Cumulative Trauma Disorders
|
Disease
|
Inferred
|
Explain
|
0.02592
|
|
61
|
Hyperhidrosis disorder
|
Disease
|
Inferred
|
Explain
|
0.02337
|
|
62
|
Tremor Adverse Event
|
Disease
|
Inferred
|
Explain
|
0.02031
|
|
63
|
Muscle Contraction
|
Function
|
Inferred
|
Explain
|
0.01931
|
|
64
|
SEPT9 gene
|
Gene
|
Inferred
|
Explain
|
0.01922
|
|
65
|
Nerve compression syndrome
|
Disease
|
Inferred
|
Explain
|
0.01921
|
|
66
|
Brachial Plexus Neuritis
|
Disease
|
Inferred
|
Explain
|
0.01715
|
|
67
|
Tremor
|
Disease
|
Inferred
|
Explain
|
0.01621
|
|
68
|
Apraxias
|
Disease
|
Inferred
|
Explain
|
0.01603
|
|
69
|
Hereditary bundle branch system defect
|
Disease
|
Inferred
|
Explain
|
0.01565
|
|
70
|
Contracture
|
Other
|
Inferred
|
Explain
|
0.01464
|
|
71
|
Familial Periodic Paralysis
|
Disease
|
Inferred
|
Explain
|
0.01414
|
|
72
|
Oculovestibuloauditory syndrome
|
Disease
|
Inferred
|
Explain
|
0.01272
|
|
73
|
SPINOCEREBELLAR ATAXIA 29
|
Disease
|
Inferred
|
Explain
|
0.01194
|
|
74
|
IGF1 gene
|
Gene
|
Inferred
|
Explain
|
0.01180
|
|
75
|
Muscular fasciculation
|
Disease
|
Inferred
|
Explain
|
0.01170
|
|
76
|
TRPV4 gene
|
Gene
|
Inferred
|
Explain
|
0.01133
|
|
77
|
SLC16A2 gene
|
Gene
|
Inferred
|
Explain
|
0.01084
|
|
78
|
CACNA1S gene
|
Gene
|
Inferred
|
Explain
|
0.01081
|
|
79
|
Ataxia as late effect of cerebrovascular disease
|
Disease
|
Inferred
|
Explain
|
0.01062
|
|
80
|
Foot
|
Other
|
Inferred
|
Explain
|
0.01061
|
|
81
|
Ataxia
|
Disease
|
Inferred
|
Explain
|
0.01033
|
|
82
|
Mononeuropathies
|
Disease
|
Inferred
|
Explain
|
0.01005
|
|
83
|
KCNE3 gene
|
Gene
|
Inferred
|
Explain
|
0.00914
|
|
84
|
Spasm
|
Disease
|
Inferred
|
Explain
|
0.00866
|
|
85
|
MILES-CARPENTER X-LINKED MENTAL RETARDATION SYNDROME
|
Disease
|
Inferred
|
Explain
|
0.00835
|
|
86
|
Tetany
|
Disease
|
Inferred
|
Explain
|
0.00829
|
|
87
|
Muscle Hypertonia
|
Disease
|
Inferred
|
Explain
|
0.00825
|
|
88
|
TTR gene
|
Gene
|
Inferred
|
Explain
|
0.00755
|
|
89
|
Muscle Cramp
|
Disease
|
Inferred
|
Explain
|
0.00741
|
|
90
|
SCN4A gene
|
Gene
|
Inferred
|
Explain
|
0.00705
|
|
91
|
Muscle Weakness
|
Disease
|
Inferred
|
Explain
|
0.00673
|
|
92
|
Mental Retardation
|
Disease
|
Inferred
|
Explain
|
0.00656
|
|
93
|
X-linked inheritance
|
Function
|
Inferred
|
Explain
|
0.00612
|
|
94
|
Peripheral Neuropathy
|
Disease
|
Inferred
|
Explain
|
0.00609
|
|
95
|
RPS6KB1 gene
|
Gene
|
Inferred
|
Explain
|
0.00599
|
|
96
|
MSTN gene
|
Gene
|
Inferred
|
Explain
|
0.00492
|
|
97
|
Sweating, Gustatory
|
Disease
|
Inferred
|
Explain
|
0.00469
|
|
98
|
biological adaptation to stress
|
Function
|
Inferred
|
Explain
|
0.00432
|
|
99
|
RUSSELL-SILVER SYNDROME, X-LINKED
|
Disease
|
Inferred
|
Explain
|
0.00409
|
|
100
|
Episodic ataxia type 1
|
Disease
|
Inferred
|
Explain
|
0.00406
|