Search results for "[genes] TRPV4"

43 hits were found for '[genes] TRPV4'

# Family MCID Name MIFTS Score
1
MTT002 Metatropic Dysplasia 37 22.513
2
SPN302 Spondylometaphyseal Dysplasia, Kozlowski Type 30 21.358
3
SCP002 Scapuloperoneal Spinal Muscular Atrophy 28 21.358
4
PRS051 Parastremmatic Dwarfism 30 20.136
5
c HRD094 Hereditary Motor and Sensory Neuropathy, Type Iic 29 18.836
6
c DGT005 Digital Arthropathy-Brachydactyly, Familial 23 18.836
7
P CHR071 Charcot-Marie-Tooth Disease 67 17.439
8
P ART023 Arthropathy 65 15.919
9
P SPN046 Spinal Muscular Atrophy 64 15.919
10
P MSC003 Muscular Atrophy 56 15.919
11
P BRC003 Brachyolmia 30 15.919
12
c BRC045 Brachyolmia Type 3 26 15.919
13
P BRC006 Brachydactyly 51 14.238
14
c PRG001 Progressive Muscular Atrophy 43 14.238
15
SDM002 Sed, Maroteaux Type 30 14.238
16
SPN303 Spinal Muscular Atrophy, Distal, Congenital Nonprogressive 24 14.238
17
P DGT007 Digital Arthropathy-Brachydactyly 12 14.238
18
TTH006 Tooth Disease 54 12.331
19
c CHR532 Charcot-Marie-Tooth Disease, Type 2e 48 12.331
20
DWR001 Dwarfism 47 12.331
21
SKL014 Skeletal Dysplasia 47 12.331
22
P AXN001 Axonal Neuropathy 38 12.331
23
c CHR139 Charcot-Marie-Tooth Disease Type 2c 21 12.331
24
NRM005 Neuromuscular Disease 60 10.068
25
PLM010 Pulmonary Edema 56 10.068
26
KNS001 Kniest Dysplasia 53 10.068
27
ACH032 Achondrogenesis, Type Ii or Hypochondrogenesis 49 10.068
28
P CHR102 Charcot-Marie-Tooth Neuropathy 48 10.068
29
MTP026 Metaphyseal Chondrodysplasia, Murk Jansen Type 48 10.068
30
SKL017 Skeletal Dysplasias 48 10.068
31
P DSB002 Desbuquois Dysplasia 46 10.068
32
OST097 Osteoporotic Fracture 45 10.068
33
HYP041 Hypochondrogenesis 45 10.068
34
BLN001 Blount's Disease 44 10.068
35
DNT007 Dentin Sensitivity 41 10.068
36
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 40 10.068
37
ACT012 Acute Hemorrhagic Conjunctivitis 39 10.068
38
SBD001 Subdural Empyema 31 10.068
39
TRP021 Trpv4-Associated Disorders 2 10.068
40
RSS002 Roussy-Levy Syndrome 51 7.119
41
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 46 7.119
42
c ATS267 Autosomal Dominant Charcot-Marie-Tooth Disease Type 2c 16 7.119
43
c ATS070 Autosomal Dominant Congenital Benign Spinal Muscular Atrophy 14 7.119