Additional Disease Briefs

Get Information about a Rare Disease

Use the form below to explore NORD's comprehensive rare disease database. Search for detailed information on rare diseases, including NORD's authoritative Rare Disease Reports and data from other reliable sources.
* = NORD Rare Disease Report

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Rare Disease Database Reports Additional Rare Disease Briefs
cone dystrophy 3

Also known as: COD3, GUCA1A cone dystrophy, cone dystrophy 3, cone dystrophy caused by mutation in GUCA1A, cone dystrophy type 3, cone dystrophy-3, cone-rod dystrophy 14, retinal cone dystrophy

cone dystrophy 4

Also known as: COD4, PDE6C cone dystrophy, achromatopsia 5, cone dystrophy 4, cone dystrophy caused by mutation in PDE6C, cone dystrophy type 4

cone dystrophy with supernormal rod response

Also known as: KCNV2-related retinopathy, RCD3B, cone dystrophy with night blindness and supernormal Rod responses, Kcnv2-related, cone dystrophy with night blindness and supernormal rod responses KCNV2 related, cone dystrophy with supernormal Rod responses, cone dystrophy with supernormal rod ERG, cone dystrophy with supernormal rod electroretinogram, cone dystrophy with supernormal rod response, cone dystrophy with supernormal scotopic electroretinogram, retinal cone dystrophy 3B, retinal cone dystrophy type 3B

cone-rod dystrophy 1

Also known as: CORD1, CRD1, Crd1, cone-rod dystrophy 1, cone-rod dystrophy type 1, cone-rod retinal dystrophy-1

cone-rod dystrophy 10

Also known as: CORD10, SEMA4A cone-rod dystrophy, cone-rod dystrophy 10, cone-rod dystrophy caused by mutation in SEMA4A, cone-rod dystrophy type 10

cone-rod dystrophy 11

Also known as: CORD11, RAX2 cone-rod dystrophy, cone-rod dystrophy 11, cone-rod dystrophy caused by mutation in RAX2, cone-rod dystrophy type 11

cone-rod dystrophy 12

Also known as: CORD12, PROM1 cone-rod dystrophy, cone-rod dystrophy 12, cone-rod dystrophy caused by mutation in PROM1, cone-rod dystrophy type 12

cone-rod dystrophy 13

Also known as: CORD13, RPGRIP1 cone-rod dystrophy, cone-rod dystrophy 13, cone-rod dystrophy caused by mutation in RPGRIP1, cone-rod dystrophy type 13

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