|
391
|
|
|
Phosphodiesterase 4D |
ACRDYS2, DPDE3, HSPDE4D, PDE43, PDE4DN2, STRK1 |
Acrodysostosis, Acrodysostosis with multiple hormone resistance, Acrodysostosis with or without hormone resistance, Asthma, Autism, Brachycephaly, Brachydactyly, Breast cancer, Breast carcinoma, Congenital craniofacial dysostosis, Congenital epicanthus, Congenital hypoplasia of radius, Congenital hypothyroidism, Cryptorchidism, Developmental delay, Diabetes mellitus, Dwarfism, Esophagus neoplasm, Haploinsufficiency syndrome, Hyperphosphatemia, Hypogonadism, Hypoplasia of the maxilla, Hypospadias, Isolated somatotropin deficiency, Kidney disease, Leukemia, Malocclusion, Melanocytic nevus, Mental depression, Mental retardation, Micromelia, Nervous system diseases, Obesity, Oral ulcer, Peripheral dysostosis, Prostatic neoplasms, Prostate cancer, Pseudohypoparathyroidism, Schizophrenia, Scoliosis, Somatotropin deficiency, Specific learning disorder, ThrombosisView all (28 more) |
|
392
|
|
|
Phosphodiesterase 6A |
CGPR-A, PDEA, RP43 |
Cataract, Congenital hypoplasia of penis, Diabetes mellitus, Disorder of eye, Glaucoma, Hearing loss, Hyperinsulinism, Hypogonadism, Keratoconus, Leber congenital amaurosis, Mental retardation, Movement disorders, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinitis pigmentosa, Rod-cone dystrophyView all (3 more) |
|
393
|
|
|
Paired related homeobox 2 |
PMX2, PRX2 |
|
|
394
|
|
|
Phosphodiesterase 6C |
ACHM5, COD4, PDEA2 |
Achromatopsia, Cone dystrophy, Cone monochromatism, Cone-rod dystrophy, Disorder of eye, Dyschromatopsia, Exotropia, Hyperopia, Nystagmus, Pendular nystagmus, Progressive cone dystrophy |
|
395
|
|
|
Phosphodiesterase 6D |
JBTS22, PDED |
Brachydactyly, Cerebellar vermis agenesis, Clinodactyly, Congenital epicanthus, Congenital heart defects, Congenital ocular coloboma, Cryptorchidism, Developmental delay, Dwarfism, Esotropia, Frontal bossing, Hearing loss, High palate, Hypoplasia of corpus callosum, Hypothalamic hamartomas, Joubert syndrome, Malformation of cortical development, Mental retardation, Micrognathism, Microphthalmos, Nystagmus, Oculomotor apraxia, Orofaciodigital syndrome, Polydactyly, Polydactyly of toes, Radial polydactyly, Renal agenesis, Renal hypoplasia, Retinal dysplasia, Syndactyly, Temporal cortical atrophy, Postaxial hand polydactylyView all (17 more) |
|
396
|
|
|
Phosphodiesterase 6G |
PDEG, RP57 |
Cataract, Congenital hypoplasia of penis, Cystoid macular edema, Diabetes mellitus, Disorder of eye, Glaucoma, Hearing loss, Hyperinsulinism, Hypogonadism, Keratoconus, Mental retardation, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinitis pigmentosa, Rod-cone dystrophyView all (2 more) |
|
397
|
|
|
Phosphodiesterase 6H |
ACHM6, RCD3 |
Achromatopsia, Color blindness, Cone dystrophy, Cone monochromatism, Cone-rod dystrophy, Disorder of eye, Dyschromatopsia, Exotropia, Hyperopia, Nyctalopia, Pendular nystagmus, Retinal cone dystrophy |
|
398
|
|
|
Phosphodiesterase 8A |
HsT19550 |
|
|
399
|
|
|
Phosphodiesterase 9A |
HSPDE9A2 |
|
|
400
|
|
|
Phosphodiesterase 1B |
HEL-S-79p, PDE1B1, PDES1B |
|
