Genes | GeDiPNet - Gene Disease Pathway & Associations

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All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

9591 to 9600 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
9591	5143	PDE4C	Phosphodiesterase 4C	DPDE1, PDE21	Gout
9592	5144	PDE4D	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)
9593	9659	PDE4DIP	Phosphodiesterase 4D interacting protein	CMYA2, MMGL	Cutaneous mastocytosis, Diabetes macrovascular complications, Mastocytosis, Scoliosis
9594	8654	PDE5A	Phosphodiesterase 5A	CGB-PDE, CN5A, PDE5	Bipolar disorder, Carotid artery disease, Endometriosis, Iga nephropathy
9595	5145	PDE6A	Phosphodiesterase 6A	CGPR-A, PDEA, RP43	Retinitis pigmentosa, Leber congenital amaurosis, Usher syndrome
9596	5158	PDE6B	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
9597	5146	PDE6C	Phosphodiesterase 6C	ACHM5, COD4, PDEA2	Achromatopsia, Amphetamine or sympathomimetic abuse, Cone dystrophy, Cone-rod dystrophy, Optic atrophy, Retinitis pigmentosa
9598	5147	PDE6D	Phosphodiesterase 6D	JBTS22, PDED	Aplasia of the vermis, Joubert syndrome, Orofaciodigital syndrome
9599	5148	PDE6G	Phosphodiesterase 6G	PDEG, RP57	Retinitis pigmentosa
9600	5149	PDE6H	Phosphodiesterase 6H	ACHM6, RCD3	Achromatopsia, Color vision deficiency, Cone dystrophy, Retinal cone dystrophy, Retinitis pigmentosa

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