×
Entrez Id:
6622
Gene Symbol:
SNCA
SNCA
0.110
GeneticVariation
phenotype
BEFREE
Age, cpRBD, chronic constipation and SNCA rs11931074 may correlate with hyposmia in Chinese PD patients.
25921825
2015
×
Entrez Id:
55248
Gene Symbol:
PACC1
PACC1
0.010
Biomarker
phenotype
BEFREE
The PAC -SYM questionnaire for chronic constipation : defining the minimal important difference.
28983926
2017
×
Entrez Id:
5047
Gene Symbol:
PAEP
PAEP
0.010
Biomarker
phenotype
BEFREE
PEG and PEG + PM are equally effective and safe in the treatment of children with chronic constipation .
28270173
2017
×
Entrez Id:
7434
Gene Symbol:
VIPR2
VIPR2
0.010
AlteredExpression
phenotype
BEFREE
VIP, VIPR1, and VIPR2 mRNA expression was significantly reduced in PD/CC vs CC and controls (P<.05).
27891695
2017
×
Entrez Id:
6863
Gene Symbol:
TAC1
TAC1
0.010
Biomarker
phenotype
BEFREE
A deficiency of the neurotransmitter substance P (SP ) has been identified in both pediatric and adult patients with chronic constipation .
16481266
2006
×
Entrez Id:
8189
Gene Symbol:
SYMPK
SYMPK
0.010
Biomarker
phenotype
BEFREE
The PAC-SYM questionnaire for chronic constipation : defining the minimal important difference.
28983926
2017
×
Entrez Id:
6523
Gene Symbol:
SLC5A1
SLC5A1
0.010
Biomarker
phenotype
BEFREE
Mizagliflozin, a novel selective SGLT1 inhibitor, exhibits potential in the amelioration of chronic constipation .
28410751
2017
×
Entrez Id:
794
Gene Symbol:
CALB2
CALB2
0.010
Biomarker
phenotype
BEFREE
Calretinin -Immunoreactive Hypoinnervation in Down Syndrome (DS): Report of an Infant with Very Short-Segment Hirschsprung Disease and Comparison to Biopsy Findings in 20 Normal Infants and 11 Infants with DS and Chronic Constipation .
26230373
2016
×
Entrez Id:
6663
Gene Symbol:
SOX10
SOX10
0.100
CausalMutation
phenotype
CLINVAR
×
Entrez Id:
8398
Gene Symbol:
PLA2G6
PLA2G6
0.100
GeneticVariation
phenotype
CLINVAR
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
0.100
CausalMutation
phenotype
CLINVAR
×
Entrez Id:
6575
Gene Symbol:
SLC20A2
SLC20A2
0.100
CausalMutation
phenotype
CLINVAR
×
Entrez Id:
5189
Gene Symbol:
PEX1
PEX1
0.100
CausalMutation
phenotype
CLINVAR
×
Entrez Id:
5813
Gene Symbol:
PURA
PURA
0.100
GeneticVariation
phenotype
CLINVAR
×
Entrez Id:
8506
Gene Symbol:
CNTNAP1
CNTNAP1
0.100
GeneticVariation
phenotype
CLINVAR
Novel mutation in CNTNAP1 results in congenital hypomyelinating neuropathy.
27668699
2017
×
Entrez Id:
57459
Gene Symbol:
GATAD2B
GATAD2B
0.100
CausalMutation
phenotype
CLINVAR
×
Entrez Id:
79876
Gene Symbol:
UBA5
UBA5
0.100
GeneticVariation
phenotype
CLINVAR
NPHP3-ACAD11
0.100
GeneticVariation
phenotype
CLINVAR
×
Entrez Id:
79876
Gene Symbol:
UBA5
UBA5
0.100
CausalMutation
phenotype
CLINVAR
×
Entrez Id:
1654
Gene Symbol:
DDX3X
DDX3X
0.100
GeneticVariation
phenotype
CLINVAR
×
Entrez Id:
4297
Gene Symbol:
KMT2A
KMT2A
0.100
CausalMutation
phenotype
CLINVAR
NPHP3-ACAD11
0.100
CausalMutation
phenotype
CLINVAR
×
Entrez Id:
5435
Gene Symbol:
POLR2F
POLR2F
0.100
CausalMutation
phenotype
CLINVAR
×
Entrez Id:
22880
Gene Symbol:
MORC2
MORC2
0.100
GeneticVariation
phenotype
CLINVAR
×
Entrez Id:
6622
Gene Symbol:
SNCA
SNCA
0.110
Biomarker
phenotype
HPO