Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "P"
271 to 280 of 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

271
Phosphodiesterase 4D
ACRDYS2, DPDE3, HSPDE4D, PDE43, PDE4DN2, STRK1
Acrodysostosis, Alzheimer disease, Amphetamine or sympathomimetic abuse, Androgenetic alopecia, Angioedema, Asthma, Breast cancer, Chromosome 5q12 deletion syndrome, Kidney disease, Color vision deficiency, Major depressive disorder, Desbuquois syndrome, Dyslexia, Esophageal atresia, Esophageal cancer
View all (15 more)

272
Phosphodiesterase 4D interacting protein
CMYA2, MMGL
Cutaneous mastocytosis, Macrovascular complications of diabetes mellitus, Mastocytosis, Scoliosis

273
Phosphodiesterase 5A
CGB-PDE, CN5A, PDE5
Bipolar disorder, Carotid artery disease, Endometriosis, Iga nephropathy

274
Phosphodiesterase 6A
CGPR-A, PDEA, RP43
Retinitis pigmentosa, Leber congenital amaurosis, Usher syndrome

275
Phosphodiesterase 6B
CSNB3, CSNBAD2, GMP-PDEbeta, PDEB, RP40, rd1
Alzheimer disease, Astrocytoma, Retinitis pigmentosa, Cone-rod dystrophy, Congenital stationary night blindness, Leber congenital amaurosis, Macular dystrophy, Night blindness, congenital stationary, Oculocutaneous albinism, Oguchi disease, Cone dystrophy, Retinal degeneration, Rod-cone dystrophy, Myopia, Diabetes mellitus, type 2

276
Phosphodiesterase 6C
ACHM5, COD4, PDEA2
Achromatopsia, Amphetamine or sympathomimetic abuse, Cone dystrophy, Cone-rod dystrophy, Optic atrophy, Retinitis pigmentosa

277
Phosphodiesterase 6D
JBTS22, PDED
Aplasia of the vermis, Joubert syndrome, Orofaciodigital syndrome

278
Phosphodiesterase 6G
PDEG, RP57
Retinitis pigmentosa

279
Phosphodiesterase 6H
ACHM6, RCD3
Achromatopsia, Color vision deficiency, Cone dystrophy, Retinal cone dystrophy, Retinitis pigmentosa

280
Phosphodiesterase 7A
HCP1, PDE7
Attention deficit hyperactivity disorder, Substance abuse