Search results for "[genes] TRPV4"

41 hits were found for '[genes] TRPV4'

# Family MCID Name MIFTS Score
1
MTT002 Metatropic Dysplasia 30 22.539
2
SPN302 Spondylometaphyseal Dysplasia, Kozlowski Type 28 21.382
3
SCP002 Scapuloperoneal Spinal Muscular Atrophy 27 21.382
4
c HRD094 Hereditary Motor and Sensory Neuropathy, Type Iic 23 21.382
5
PRS051 Parastremmatic Dwarfism 25 20.159
6
c DGT005 Digital Arthropathy-Brachydactyly, Familial 35 18.857
7
P BRC045 Brachyolmia Type 3 33 18.857
8
P CHR071 Charcot-Marie-Tooth Disease 66 17.458
9
SPN303 Spinal Muscular Atrophy, Distal, Congenital Nonprogressive 23 17.458
10
P ART023 Arthropathy 63 15.937
11
P SPN046 Spinal Muscular Atrophy 63 15.937
12
P MSC003 Muscular Atrophy 51 15.937
13
P BRC006 Brachydactyly 52 14.255
14
SKL014 Skeletal Dysplasia 46 14.255
15
c PRG001 Progressive Muscular Atrophy 40 14.255
16
SDM002 Sed, Maroteaux Type 26 14.255
17
c CHR139 Charcot-Marie-Tooth Disease Type 2c 21 14.255
18
P DGT007 Digital Arthropathy-Brachydactyly 10 14.255
19
NRM005 Neuromuscular Disease 57 12.345
20
PLM010 Pulmonary Edema 56 12.345
21
TTH006 Tooth Disease 52 12.345
22
DWR001 Dwarfism 46 12.345
23
P AXN001 Axonal Neuropathy 38 12.345
24
KNS001 Kniest Dysplasia 53 10.080
25
P DSB006 Desbuquois Dysplasia 1 53 10.080
26
P MGL002 Megalencephalic Leukoencephalopathy with Subcortical Cysts 51 10.080
27
ACH032 Achondrogenesis, Type Ii or Hypochondrogenesis 51 10.080
28
c CHR532 Charcot-Marie-Tooth Disease, Type 2e 47 10.080
29
MTP026 Metaphyseal Chondrodysplasia, Murk Jansen Type 45 10.080
30
SKL017 Skeletal Dysplasias 45 10.080
31
P CHR102 Charcot-Marie-Tooth Neuropathy 43 10.080
32
BLN001 Blount's Disease 42 10.080
33
HYP041 Hypochondrogenesis 40 10.080
34
DNT007 Dentin Sensitivity 38 10.080
35
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 37 10.080
36
SBD001 Subdural Empyema 30 10.080
37
c BRC053 Brachyolmia Type 2 18 10.080
38
TRP021 Trpv4-Associated Disorders 2 10.080
39
RSS002 Roussy-Levy Syndrome 52 7.127
40
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 51 7.127
41
c CHR520 Charcot-Marie-Tooth Disease, Axonal, Type 2s 36 7.127