cone-rod dystrophy
retinal degeneration that characterized by progressive deterioration of the cone and rod photoreceptor cells
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cone-rod dystrophy
Summary
cone-rod dystrophy is a class of disease[1].
Key Facts
- cone-rod dystrophy's instance of is recorded as class of disease[2].
- cone-rod dystrophy's subclass of is recorded as retinal degeneration[3].
- cone-rod dystrophy's subclass of is recorded as monogenic disease[4].
- cone-rod dystrophy's MeSH descriptor ID is recorded as D000071700[5].
- cone-rod dystrophy's KEGG ID is recorded as H00481[6].
- cone-rod dystrophy's MeSH tree code is recorded as C11.270.152[7].
- cone-rod dystrophy's MeSH tree code is recorded as C11.768.585.658.250[8].
- cone-rod dystrophy's MeSH tree code is recorded as C16.320.290.152[9].
- cone-rod dystrophy's Disease Ontology ID is recorded as DOID:0050572[10].
- cone-rod dystrophy's Orphanet ID is recorded as 1872[11].
- cone-rod dystrophy's health specialty is recorded as ophthalmology[12].
- cone-rod dystrophy's health specialty is recorded as medical genetics[13].
- cone-rod dystrophy's genetic association is recorded as PROM1[14].
- cone-rod dystrophy's genetic association is recorded as LOC118142757[15].
- cone-rod dystrophy's genetic association is recorded as RPGRIP1[16].
- cone-rod dystrophy's genetic association is recorded as PDE6C[17].
- cone-rod dystrophy's genetic association is recorded as CACNA1F[18].
- cone-rod dystrophy's genetic association is recorded as CRX[19].
- cone-rod dystrophy's genetic association is recorded as GUCY2D[20].
- cone-rod dystrophy's genetic association is recorded as POC1B[21].
- cone-rod dystrophy's genetic association is recorded as CDHR1[22].
- cone-rod dystrophy's genetic association is recorded as DRAM2[23].
- cone-rod dystrophy's genetic association is recorded as CFAP418[24].
- cone-rod dystrophy's genetic association is recorded as RPGR[25].
- cone-rod dystrophy's genetic association is recorded as ABCA4[26].