PDE4D, phosphodiesterase 4D, 5144

N. diseases: 210; N. variants: 68
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0220659
Disease: Acrodysostosis
Acrodysostosis
0.700 GeneticVariation disease BEFREE PRKAR1A and PDE4D mutations cause acrodysostosis but two distinct syndromes with or without GPCR-signaling hormone resistance. 23043190 2012
CUI: C0220659
Disease: Acrodysostosis
Acrodysostosis
0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C0220659
Disease: Acrodysostosis
Acrodysostosis
0.700 Biomarker disease CTD_human
ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE
0.500 Biomarker disease GENOMICS_ENGLAND Identification of novel mutations confirms PDE4D as a major gene causing acrodysostosis. 23033274 2013
CUI: C0011570
Disease: Mental Depression
Mental Depression
0.500 Biomarker disease RGD The rat model confirms Pde4d's role in depression but not in spatial learning or memory enhancement and shows for the first time higher fear conditioning and altered extinction compared with controls. 22487514 2012
CUI: C0011570
Disease: Mental Depression
Mental Depression
0.500 Biomarker disease PSYGENET The rat model confirms Pde4d's role in depression but not in spatial learning or memory enhancement and shows for the first time higher fear conditioning and altered extinction compared with controls. 22487514 2012
CUI: C0011570
Disease: Mental Depression
Mental Depression
0.500 Biomarker disease PSYGENET These results suggest that PDE4D is an essential mediator of the antidepressant-like effects of rolipram, and that PDE4D-regulated cyclic adenosine monophosphate signaling may play a role in the pathophysiology and pharmacotherapy of depression. 12377395 2002
ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE
0.500 Biomarker disease CTD_human
CUI: C0004096
Disease: Asthma
Asthma
0.470 GeneticVariation disease BEFREE Two SNPs, rs1544791 (PDE4D) and rs3806932 (TSLP), were more strongly associated with the high smoking history subgroup than with asthma or any other subgroups. 27058054 2016
CUI: C0004096
Disease: Asthma
Asthma
0.470 GeneticVariation disease BEFREE Our rank-based genome-wide analysis revealed for the first time an association of RYR2 variants with asthma and replicated previously discovered PDE4D asthma gene across human populations. 23829686 2013
CUI: C0004096
Disease: Asthma
Asthma
0.470 Biomarker disease BEFREE An important genetic component to asthma susceptibility has long been recognized, most recently through the identification of several genes (e.g., ORMDL3, PDE4D, HLA-DQ, and TLE4) via genome-wide association studies. 23181788 2012
CUI: C0004096
Disease: Asthma
Asthma
0.470 Biomarker disease BEFREE Long-acting β(2)-agonists are now contraindicated as monotherapy for asthma, and increased PDE4D has been speculated to contribute to this phenomenon. 22101762 2012
CUI: C0004096
Disease: Asthma
Asthma
0.470 GeneticVariation disease GWASDB Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. 21907864 2011
CUI: C0004096
Disease: Asthma
Asthma
0.470 Biomarker disease CTD_human β2-Agonist induced cAMP is decreased in asthmatic airway smooth muscle due to increased PDE4D. 21611147 2011
CUI: C0004096
Disease: Asthma
Asthma
0.470 GeneticVariation disease BEFREE We sought to search for new variants associated with asthma and attempt to replicate the association with four loci reported previously (ORMDL3, PDE4D, DENND1B and IL1RL1). 21150878 2011
CUI: C0004096
Disease: Asthma
Asthma
0.470 Biomarker disease BEFREE Gene-based analyses that included all available SNPs in each gene found associations (P < .05) with both phenotypes for several genes: neuronal growth regulator 1 (NEGR1); roundabout, axon guidance receptor, homolog 1 (ROBO1); diacylglycerol kinase, gamma (DGKG); Fas apoptotic inhibitory molecule 2 (FAIM2); fat mass and obesity associated (FTO); and carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 8 (CHST8) among the BMI GWAS genes; interleukin 1 receptor-like 1 / interleukin 18 receptor 1 (IL1RL1/IL18R1), dipeptidyl-peptidase 10 (DPP10), phosphodiesterase 4D (PDE4D), V-myb myeloblastosis viral oncogene homolog (MYB), PDE10A, IL33, and especially protein tyrosine phosphatase, receptor type D (PTPRD) among the asthma GWAS genes; and protein kinase C, alpha (PRKCA) among the BMI and asthma candidate genes. 20816195 2010
CUI: C0004096
Disease: Asthma
Asthma
0.470 GeneticVariation disease GWASDB Asthma-susceptibility variants identified using probands in case-control and family-based analyses. 20698975 2010
CUI: C0004096
Disease: Asthma
Asthma
0.470 GeneticVariation disease GWASDB The phosphodiesterase 4D, cAMP-specific (phosphodiesterase E3 dunce homolog, Drosophila) gene (PDE4D) is a regulator of airway smooth-muscle contractility, and PDE4 inhibitors have been developed as medications for asthma. 19426955 2009
CUI: C0004096
Disease: Asthma
Asthma
0.470 Biomarker disease CTD_human The phosphodiesterase 4D, cAMP-specific (phosphodiesterase E3 dunce homolog, Drosophila) gene (PDE4D) is a regulator of airway smooth-muscle contractility, and PDE4 inhibitors have been developed as medications for asthma. 19426955 2009
CUI: C0004096
Disease: Asthma
Asthma
0.470 Biomarker disease BEFREE The phosphodiesterase 4D, cAMP-specific (phosphodiesterase E3 dunce homolog, Drosophila) gene (PDE4D) is a regulator of airway smooth-muscle contractility, and PDE4 inhibitors have been developed as medications for asthma. 19426955 2009
CUI: C0004096
Disease: Asthma
Asthma
0.470 GeneticVariation disease GWASCAT The phosphodiesterase 4D, cAMP-specific (phosphodiesterase E3 dunce homolog, Drosophila) gene (PDE4D) is a regulator of airway smooth-muscle contractility, and PDE4 inhibitors have been developed as medications for asthma. 19426955 2009
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.420 GeneticVariation disease BEFREE We identified 4570 SNPs across the PDE4D gene, with 380 associated to schizophrenia (p ≤ 0.05). 31138891 2019
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.420 GeneticVariation disease GWASDB Genome-wide association study identifies five new schizophrenia loci. 21926974 2011
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.420 Biomarker disease PSYGENET Greater significance was observed with allelic haplotypes of PDE4D (p = .00084), PDE4B (p = .0022 and p = .029), and NDEL1 (p = .0027) that increased or decreased schizophrenia susceptibility. 19251251 2009
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.420 GeneticVariation disease BEFREE Greater significance was observed with allelic haplotypes of PDE4D (p = .00084), PDE4B (p = .0022 and p = .029), and NDEL1 (p = .0027) that increased or decreased schizophrenia susceptibility. 19251251 2009