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Results 1 - 10 of 40 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. 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
  4. 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
  5. 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
  6. 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
  7. 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
  8. Vitelliform macular dystrophy 
    ... 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/.../condition/vitelliform-macular-dystrophy - Genetics
  9. CRX gene 
    ... This Health Condition MedlinePlus Genetics provides information about Retinitis pigmentosa More About This Health Condition cone-rod homeobox protein CORD2 CRD LCA7 orthodenticle homeobox 3 OTX3 Tests of CRX PubMed CONE-ROD HOMEOBOX- ...
    https://medlineplus.gov/genetics/gene/crx - Genetics
  10. Usher syndrome 
    ... of the eye (cataracts). However, many people with retinitis pigmentosa retain some central vision throughout their lives.Researchers have identified three major types of Usher syndrome, designated as types ...
    https://medlineplus.gov/genetics/condition/usher-syndrome - Genetics
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