cone-rod dystrophy
retinal degeneration that characterized by progressive deterioration of the cone and rod photoreceptor cells
Facts
7 properties- Instance of
- class of disease
- Subclass of
- retinal degeneration, monogenic disease[2][3]
- Age of onset
- juvenile onset, adult onset, childhood onset[21][22][23]
- Genetic association
- PROM1, LOC118142757, RPGRIP1, PDE6C, CACNA1F, CRX, GUCY2D, POC1B, CDHR1, DRAM2, CFAP418, RPGR, ABCA4, ADAM9, AIPL1, ATF6, CFAP410, CNGA3, OPN1MW, RAB28, OPN1LW, PRPH2, RLBP1, SEMA4A, UNC119, RIMS1, NMNAT1, RAX2, TTLL5, CACNA2D4, PITPNM3, TLCD3B, MFSD8, UBAP1L[7][8][9][10][11][12][13][14][15][16][17][18][19][20]
- Health specialty
- ophthalmology, medical genetics[5][6]
- On focus list of Wikimedia project
- WikiProject Medicine[24]
- Prevalence
- +0.00005[4]
🏷️ Also known as
en cone-rod dystrophy
en cone-rod dystrophy 5
en cone-rod retinal dystrophy
fr dystrophie des cônes et des bâtonnets
🔖 Identifiers · 10
- Disease Ontology ID
- DOID:0050572
- Exact match
- purl.obolibrary.org, identifiers.org, www.orpha.net
- GARD rare disease ID
- 10790
- ICD-10-CM
- H35.5
- ICD-11 ID (Foundation)
- 2109196114
- KEGG ID
- H00481
- MeSH descriptor ID
- D000071700
- MeSH tree code
- C11.270.152, C11.768.585.658.250, C16.320.290.152
- Orphanet ID
- 1872
- Raras disease ID
- D01872
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Summary
cone-rod dystrophy is a class of disease[1].