Results 1 - 10 of 67 for "Cone-rod" dystrophy 3
  1. ... Registry: Cone-rod dystrophy 20 Genetic Testing Registry: Cone-rod dystrophy 3 Genetic Testing Registry: Cone-rod dystrophy 5 Genetic ... X-linked 1 Genetic Testing Registry: X-linked cone-rod dystrophy 3 Cone-rod dystrophy Disease InfoSearch National Organization for ...
  2. ... body. COD1 CORDX1 CRD PCDX retinitis pigmentosa 15 retinitis pigmentosa 3 GTPase regulator RP15 RP3 RPGR_HUMAN X-linked retinitis pigmentosa GTPase regulator XLRP3 Tests of RPGR PubMed CONE- ...
  3. Usher Syndrome (National Library of Medicine)  
    ... inherited disease that causes serious hearing loss and retinitis pigmentosa, an eye disorder that causes your vision to get worse over time. It is the most common condition that affects both hearing and vision. There are three types of Usher syndrome: People with type I ...
  4. ... DISEASE CALCIUM CHANNEL, VOLTAGE-DEPENDENT, ALPHA-1F SUBUNIT CONE-ROD DYSTROPHY, X-LINKED, 3 ClinVar NCBI Gene Bech-Hansen NT, Naylor MJ, ...
  5. ... Nakamura M, Ohnishi Y, Miyake Y. Autosomal dominant cone-rod dystrophy with R838H and R838C mutations in the GUCY2D gene in Japanese patients. Jpn J Ophthalmol. 2004 May-Jun;48(3):228-35. Citation on PubMed Kitiratschky VB, Wilke ...
  6. ... Traboulsi EI. Update on the molecular genetics of retinitis pigmentosa. Ophthalmic Genet. 2001 Sep;22(3):133-54. Review. Citation on PubMed Wells J, ... retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular ... Nat Genet. 1993 Mar;3(3):213-8. Citation on PubMed Yang Z, ...
  7. ... photoreceptors underlies the progressive vision loss characteristic of retinitis pigmentosa. More About This Health Condition DELXp11.3 KIAA0215 NM23-H10 NME10 protein XRP2 retinitis pigmentosa ...
  8. Retinitis Pigmentosa (Foundation Fighting Blindness)  
    Usher Syndrome/Learn More ... Usher Syndrome ... Retinal Disorders/Specifics ... Retinal Disorders ... Foundation Fighting Blindness ... What is Retinitis Pigmentosa? Learn about ...
  9. ... This Health Condition MedlinePlus Genetics provides information about Cone-rod dystrophy More About This Health Condition ACHM5 cGMP phosphodiesterase 6C COD4 cone cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha' PDEA2 phosphodiesterase 6C, ...
  10. Bardet-Biedl Syndrome (Foundation Fighting Blindness)  
    Birth Defects/Specifics ... Birth Defects ... Retinal Disorders/Specifics ... Retinal Disorders ... Foundation Fighting Blindness ... What is Bardet Biedl Syndrome? Learn about ...
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · next