Search results for "[genes] TRPV4"

50 hits were found for '[genes] TRPV4'

# Family MCID Name MIFTS Score
1
c HRD094 Hereditary Motor and Sensory Neuropathy, Type Iic 34 21.974
2
MTT002 Metatropic Dysplasia 30 21.974
3
SPN302 Spondylometaphyseal Dysplasia, Kozlowski Type 27 20.847
4
SCP002 Scapuloperoneal Spinal Muscular Atrophy 27 20.847
5
PRS051 Parastremmatic Dwarfism 24 19.654
6
c BRC045 Brachyolmia Type 3 34 18.385
7
c DGT005 Digital Arthropathy-Brachydactyly, Familial 33 18.385
8
SPN303 Spinal Muscular Atrophy, Distal, Congenital Nonprogressive 23 18.385
9
P CHR071 Charcot-Marie-Tooth Disease 67 17.021
10
SDM002 Sed, Maroteaux Type 26 17.021
11
P BRC003 Brachyolmia 25 17.021
12
P SPN046 Spinal Muscular Atrophy 65 15.538
13
P ART023 Arthropathy 64 15.538
14
P MSC003 Muscular Atrophy 50 15.538
15
P NRP001 Neuropathy 59 13.898
16
PLM010 Pulmonary Edema 54 13.898
17
SKL014 Skeletal Dysplasia 46 13.898
18
c PRG001 Progressive Muscular Atrophy 39 13.898
19
P AXN001 Axonal Neuropathy 38 13.898
20
c CHR139 Charcot-Marie-Tooth Disease Type 2c 21 13.898
21
c BRC053 Brachyolmia Type 2 18 13.898
22
P DGT007 Digital Arthropathy-Brachydactyly 10 13.898
23
NRM005 Neuromuscular Disease 56 12.036
24
KNS001 Kniest Dysplasia 53 12.036
25
TTH006 Tooth Disease 52 12.036
26
ACH032 Achondrogenesis, Type Ii or Hypochondrogenesis 51 12.036
27
P MGL002 Megalencephalic Leukoencephalopathy with Subcortical Cysts 51 12.036
28
RSS002 Roussy-Levy Syndrome 50 12.036
29
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 49 12.036
30
c CHR532 Charcot-Marie-Tooth Disease, Type 2e 49 12.036
31
SKL017 Skeletal Dysplasias 45 12.036
32
MTP026 Metaphyseal Chondrodysplasia, Murk Jansen Type 44 12.036
33
P DSB002 Desbuquois Dysplasia 43 12.036
34
BLN001 Blount's Disease 41 12.036
35
HYP041 Hypochondrogenesis 38 12.036
36
c CHR520 Charcot-Marie-Tooth Disease, Axonal, Type 2s 36 12.036
37
DNT007 Dentin Sensitivity 35 12.036
38
SBD001 Subdural Empyema 30 12.036
39
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 30 12.036
40
TRP021 Trpv4-Associated Disorders 2 12.036
41
c DSB006 Desbuquois Dysplasia 1 50 9.827
42
c CHR376 Charcot-Marie-Tooth Disease, Type 4d 42 9.827
43
c CHR350 Charcot-Marie-Tooth Disease, Axonal, Type 2k 36 9.827
44
c DFN189 Deafness, Autosomal Dominant 25 33 9.827
45
c CHR351 Charcot-Marie-Tooth Disease, Axonal, Type 2n 31 9.827
46
c ALZ033 Alzheimer Disease 19, Late Onset 30 9.827
47
P BCK002 Beckwith-Wiedemann Syndrome 56 6.949
48
P AVS004 Avascular Necrosis of the Femoral Head 56 6.949
49
TLP001 Talipes Equinovarus 38 6.949
50
CLB019 Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly 24 6.949