Search results for "[genes] TRPV4"

43 hits were found for '[genes] TRPV4'

# Family MCID Name MIFTS Score
1
MTT002 Metatropic Dysplasia 35 22.513
2
SPN302 Spondylometaphyseal Dysplasia, Kozlowski Type 32 21.358
3
SCP002 Scapuloperoneal Spinal Muscular Atrophy 29 21.358
4
PRS051 Parastremmatic Dwarfism 31 20.136
5
c DGT005 Digital Arthropathy-Brachydactyly, Familial 25 18.836
6
c HRD094 Hereditary Motor and Sensory Neuropathy, Type Iic 24 18.836
7
P CHR071 Charcot-Marie-Tooth Disease 58 17.439
8
P SPN046 Spinal Muscular Atrophy 54 15.919
9
P ART023 Arthropathy 51 15.919
10
P MSC003 Muscular Atrophy 42 15.919
11
c BRC045 Brachyolmia Type 3 28 15.919
12
P BRC003 Brachyolmia 28 15.919
13
P BRC006 Brachydactyly 49 14.238
14
c PRG001 Progressive Muscular Atrophy 35 14.238
15
SDM002 Sed, Maroteaux Type 31 14.238
16
SPN303 Spinal Muscular Atrophy, Distal, Congenital Nonprogressive 26 14.238
17
P DGT007 Digital Arthropathy-Brachydactyly 10 14.238
18
c CHR532 Charcot-Marie-Tooth Disease, Type 2e 47 12.331
19
TTH006 Tooth Disease 43 12.331
20
SKL014 Skeletal Dysplasia 40 12.331
21
DWR001 Dwarfism 36 12.331
22
P AXN001 Axonal Neuropathy 32 12.331
23
c CHR139 Charcot-Marie-Tooth Disease Type 2c 24 12.331
24
KNS001 Kniest Dysplasia 53 10.068
25
ACH032 Achondrogenesis, Type Ii or Hypochondrogenesis 50 10.068
26
MTP026 Metaphyseal Chondrodysplasia, Murk Jansen Type 46 10.068
27
PLM010 Pulmonary Edema 45 10.068
28
NRM005 Neuromuscular Disease 44 10.068
29
HYP041 Hypochondrogenesis 44 10.068
30
P DSB002 Desbuquois Dysplasia 42 10.068
31
BLN001 Blount's Disease 39 10.068
32
OST097 Osteoporotic Fracture 37 10.068
33
SKL017 Skeletal Dysplasias 37 10.068
34
ACT012 Acute Hemorrhagic Conjunctivitis 35 10.068
35
P CHR102 Charcot-Marie-Tooth Neuropathy 35 10.068
36
SBD001 Subdural Empyema 32 10.068
37
DNT007 Dentin Sensitivity 32 10.068
38
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 27 10.068
39
TRP021 Trpv4-Associated Disorders 2 10.068
40
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 48 7.119
41
RSS002 Roussy-Levy Syndrome 43 7.119
42
c ATS267 Autosomal Dominant Charcot-Marie-Tooth Disease Type 2c 14 7.119
43
c ATS070 Autosomal Dominant Congenital Benign Spinal Muscular Atrophy 13 7.119