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Results 1 - 10 of 71 for "Cone-rod" dystrophy 3
  1. Cone-rod dystrophy 
    ... Registry: Cone-rod dystrophy 20 Genetic Testing Registry: Cone-rod dystrophy 3 Genetic Testing Registry: Cone-rod dystrophy 5 Genetic ... rod dystrophy 1 Genetic Testing Registry: X-linked cone-rod dystrophy 3 Cone rod dystrophy National Organization for Rare Disorders ( ...
    https://medlineplus.gov/genetics/condition/cone-rod-dystrophy - Genetics
  2. RPGR gene 
    ... 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 RETINITIS ...
    https://medlineplus.gov/genetics/gene/rpgr - Genetics
  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 ...
    https://medlineplus.gov/ushersyndrome.html - Health Topics
  4. CACNA1F gene 
    ... CALCIUM CHANNEL, VOLTAGE-DEPENDENT, ALPHA-1F SUBUNIT; CACNA1F CONE-ROD DYSTROPHY, X-LINKED, 3; CORDX3 ALAND ISLAND EYE DISEASE; AIED NCBI Gene ...
    https://medlineplus.gov/genetics/gene/cacna1f - Genetics
  5. PRPH2 gene 
    ... Traboulsi EI. Update on the molecular genetics of retinitis pigmentosa. Ophthalmic Genet. 2001 Sep;22(3):133-54. doi: 10.1076/opge.22.3. ... retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy. Nat Genet. 1993 Mar;3(3):213-8. doi: 10.1038/ng0393-213. ...
    https://medlineplus.gov/genetics/gene/prph2 - Genetics
  6. RP2 gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/rp2 - Genetics
  7. GUCY2D gene 
    ... 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. doi: 10.1007/s10384-003-0050- ...
    https://medlineplus.gov/genetics/gene/gucy2d - Genetics
  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 ...
    https://www.fightingblindness.org/diseases/retinitis-pigmentosa - External Health Links
  9. PDE6C gene 
    ... 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, ...
    https://medlineplus.gov/genetics/gene/pde6c - Genetics
  10. Bardet-Biedl Syndrome (Foundation Fighting Blindness)  
    Birth Defects/Specifics ... Birth Defects ... Retinal Disorders/Specifics ... Retinal Disorders ... What is Bardet Biedl Syndrome? Learn about the signs and symptoms of the ...
    https://www.fightingblindness.org/diseases/bardet-biedl-syndrome-bbs - External Health Links
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