Search results for "[genes] TRPV4"

42 hits were found for '[genes] TRPV4'

# Family MCID Name MIFTS Score
1
MTT002 Metatropic Dysplasia 32 22.471
2
SCP002 Scapuloperoneal Spinal Muscular Atrophy 30 21.318
3
SPN302 Spondylometaphyseal Dysplasia, Kozlowski Type 32 21.318
4
PRS051 Parastremmatic Dwarfism 29 20.099
5
c HRD094 Hereditary Motor and Sensory Neuropathy, Type Iic 24 20.099
6
c DGT005 Digital Arthropathy-Brachydactyly, Familial 36 18.801
7
SPN303 Spinal Muscular Atrophy, Distal, Congenital Nonprogressive 27 17.406
8
P CHR071 Charcot-Marie-Tooth Disease 66 15.890
9
P SPN046 Spinal Muscular Atrophy 62 15.890
10
P ART023 Arthropathy 63 15.890
11
c BRC045 Brachyolmia Type 3 28 15.890
12
P MSC003 Muscular Atrophy 51 15.890
13
P BRC003 Brachyolmia 26 15.890
14
SDM002 Sed, Maroteaux Type 29 14.212
15
c CHR139 Charcot-Marie-Tooth Disease Type 2c 22 14.212
16
P BRC006 Brachydactyly 53 14.212
17
c PRG001 Progressive Muscular Atrophy 39 14.212
18
SKL014 Skeletal Dysplasia 44 14.212
19
P DGT007 Digital Arthropathy-Brachydactyly 10 14.212
20
c CHR532 Charcot-Marie-Tooth Disease, Type 2e 45 12.308
21
NRM005 Neuromuscular Disease 56 12.308
22
TTH006 Tooth Disease 52 12.308
23
PLM010 Pulmonary Edema 56 12.308
24
DWR001 Dwarfism 42 12.308
25
P CHR102 Charcot-Marie-Tooth Neuropathy 43 12.308
26
P AXN001 Axonal Neuropathy 37 12.308
27
P MGL002 Megalencephalic Leukoencephalopathy with Subcortical Cysts 50 10.050
28
ACH032 Achondrogenesis, Type Ii or Hypochondrogenesis 51 10.050
29
KNS001 Kniest Dysplasia 52 10.050
30
MTP026 Metaphyseal Chondrodysplasia, Murk Jansen Type 46 10.050
31
BLN001 Blount's Disease 46 10.050
32
ACT012 Acute Hemorrhagic Conjunctivitis 37 10.050
33
HYP041 Hypochondrogenesis 40 10.050
34
P DSB002 Desbuquois Dysplasia 42 10.050
35
DNT007 Dentin Sensitivity 35 10.050
36
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 36 10.050
37
SBD001 Subdural Empyema 30 10.050
38
SKL017 Skeletal Dysplasias 41 10.050
39
TRP021 Trpv4-Associated Disorders 2 10.050
40
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 48 7.106
41
RSS002 Roussy-Levy Syndrome 51 7.106
42
c BRC053 Brachyolmia Type 2 18 7.106