- autosomal dominant retinitis pigmentosa
- 常染色体显性色素性视网膜炎
Medical Chinese dictionary (湘雅医学词典). 2013.
autosomal dominant retinitis pigmentosa
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Retinitis pigmentosa — DiseaseDisorder infobox Name = Retinitis pigmentosa ICD10 = ICD10|H|35|5|h|30 ICD9 = ICD9|362.74 OMIM = 268000 MeshID = D012174Retinitis pigmentosa (RP) is a group of genetic eye conditions. In the progression of symptoms for RP, night blindness… … Wikipedia
retinitis — Inflammation of the retina. [retina + G. itis, inflammation] albuminuric r. hypertensive retinopathy. circinate r. circinate retinopathy. diabetic r. diabetic retinopathy … Medical dictionary
RP1 — Retinitis pigmentosa 1 (autosomal dominant), also known as RP1, is a human gene.cite web | title = Entrez Gene: RP1 retinitis pigmentosa 1 (autosomal dominant)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… … Wikipedia
RP9 — Retinitis pigmentosa 9 (autosomal dominant) Identifiers Symbols RP9; PAP 1 External IDs … Wikipedia
Rhodopsin — Rhodopsin, also known as visual purple, is a pigment of the retina that is responsible for both the formation of the photoreceptor cells and the first events in the perception of light. Rhodopsins belong to the G protein coupled receptor family… … Wikipedia
Peripherin 2 — (retinal degeneration, slow), also known as PRPH2, is a human gene.cite web | title = Entrez Gene: PRPH2 peripherin 2 (retinal degeneration, slow)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=5961|… … Wikipedia
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PDE6B — Phosphodiesterase 6B, cGMP specific, rod, beta Identifiers Symbols PDE6B; CSNB3; CSNBAD2; PDEB; RP40; rd1 External IDs … Wikipedia
PRPF3 — PRP3 pre mRNA processing factor 3 homolog (S. cerevisiae), also known as PRPF3, is a human gene.cite web | title = Entrez Gene: PRPF3 PRP3 pre mRNA processing factor 3 homolog (S. cerevisiae)| url =… … Wikipedia
PRPF8 — PRP8 pre mRNA processing factor 8 homolog (S. cerevisiae), also known as PRPF8, is a human gene. PBB Summary section title = summary text = Pre mRNA splicing occurs in 2 sequential transesterification steps. The protein encoded by this gene is a… … Wikipedia
FSCN2 — Fascin homolog 2, actin bundling protein, retinal (Strongylocentrotus purpuratus), also known as FSCN2, is a human gene.cite web | title = Entrez Gene: FSCN2 fascin homolog 2, actin bundling protein, retinal (Strongylocentrotus purpuratus)| url … Wikipedia
