Search results for "[genes] TRPV4"

42 hits were found for '[genes] TRPV4'

# Family MCID Name MIFTS Score
1
MTT002 Metatropic Dysplasia 40 22.572
2
SPN302 Spondylometaphyseal Dysplasia, Kozlowski Type 34 21.414
3
SCP002 Scapuloperoneal Spinal Muscular Atrophy 31 21.414
4
P CHR071 Charcot-Marie-Tooth Disease 59 20.189
5
PRS051 Parastremmatic Dwarfism 31 20.189
6
c HRD094 Hereditary Motor and Sensory Neuropathy, Type Iic 29 18.885
7
c DGT005 Digital Arthropathy-Brachydactyly, Familial 27 18.885
8
P NRP001 Neuropathy 48 17.485
9
P SPN046 Spinal Muscular Atrophy 58 15.961
10
P ART023 Arthropathy 50 15.961
11
P MSC003 Muscular Atrophy 45 15.961
12
c BRC045 Brachyolmia Type 3 30 15.961
13
P BRC003 Brachyolmia 23 15.961
14
P BRC006 Brachydactyly 48 14.276
15
SDM002 Sed, Maroteaux Type 33 14.276
16
c PRG001 Progressive Muscular Atrophy 33 14.276
17
SPN303 Spinal Muscular Atrophy, Distal, Congenital Nonprogressive 28 14.276
18
P DGT007 Digital Arthropathy-Brachydactyly 11 14.276
19
c CHR532 Charcot-Marie-Tooth Disease, Type 2e 48 12.363
20
TTH006 Tooth Disease 47 12.363
21
PLM010 Pulmonary Edema 45 12.363
22
DWR001 Dwarfism 42 12.363
23
SKL014 Skeletal Dysplasia 38 12.363
24
P AXN001 Axonal Neuropathy 35 12.363
25
c CHR139 Charcot-Marie-Tooth Disease Type 2c 23 12.363
26
KNS001 Kniest Dysplasia 55 10.095
27
ACH032 Achondrogenesis, Type Ii or Hypochondrogenesis 51 10.095
28
P MGL002 Megalencephalic Leukoencephalopathy with Subcortical Cysts 50 10.095
29
MTP026 Metaphyseal Chondrodysplasia, Murk Jansen Type 46 10.095
30
BLN001 Blount's Disease 41 10.095
31
SKL017 Skeletal Dysplasias 39 10.095
32
ACT012 Acute Hemorrhagic Conjunctivitis 37 10.095
33
HYP041 Hypochondrogenesis 36 10.095
34
OST097 Osteoporotic Fracture 35 10.095
35
SBD001 Subdural Empyema 31 10.095
36
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 28 10.095
37
DNT007 Dentin Sensitivity 27 10.095
38
TRP021 Trpv4-Associated Disorders 2 10.095
39
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 52 7.138
40
RSS002 Roussy-Levy Syndrome 46 7.138
41
c ATS267 Autosomal Dominant Charcot-Marie-Tooth Disease Type 2c 15 7.138
42
c ATS070 Autosomal Dominant Congenital Benign Spinal Muscular Atrophy 14 7.138