Retinitis Pigmentosa 66; Rp66

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Retinitis Pigmentosa 66; Rp66

RBP3

View recommended genes panels

Clinical Features

Top most frequent phenotypes and symptoms related to Retinitis Pigmentosa 66; Rp66

Cataract
Edema
Blindness
Rod-cone dystrophy
Reduced visual acuity
Pallor
Nyctalopia
Confusion
Optic disc pallor
Constriction of peripheral visual field

And another 6 symptoms. If you need more information about this disease we can help you.

Click here to know more about Mendelian.

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Retinitis Pigmentosa 66; Rp66 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
RBP3 Deletion/Duplication Analysis. By Baylor Miraca Genetics Laboratories (United States). RBP3 Specificity 100 % Genes 100 %
RBP3 Comprehensive - Sequence & Deletion/Duplication Analysis. By Baylor Miraca Genetics Laboratories (United States). RBP3 Specificity 100 % Genes 100 %
RBP3 Sequence Analysis. By Baylor Miraca Genetics Laboratories (United States). RBP3 Specificity 100 % Genes 100 %
RBP3 Sequence Analysis (Prenatal Diagnosis). By Baylor Miraca Genetics Laboratories (United States). RBP3 Specificity 100 % Genes 100 %
RBP3. By Institute for Human Genetics University Clinic Freiburg (Germany). RBP3 Specificity 100 % Genes 100 %
Retinitis pigmentosa 66 (sequence analysis of RBP3 gene). By CGC Genetics (Portugal). RBP3 Specificity 100 % Genes 100 %
Retinitis pigmentosa (NGS panel for 72 genes). By CGC Genetics (Portugal). RHO, RLBP1, ROM1, RP1, RP2, RP9, RPE65, RPGR, SAG, SEMA4A, TUB, TULP1, USH2A, CLRN1, BEST1, ARL6, CA4, ADGRA3, PRPF31, KLHL7 , (...) View the complete list with 52 more genes Panel complete gene list RHO, RLBP1, ROM1, RP1, RP2, RP9, RPE65, RPGR, SAG, SEMA4A, TUB, TULP1, USH2A, CLRN1, BEST1, ARL6, CA4, ADGRA3, PRPF31, KLHL7, PRPF6, RP1L1, ARL2BP, DHX38, PRPF8, PRPF3, PRPF4, NMNAT1, RDH11, IMPG2, RDH12, TTC8, SPATA7, DHDDS, CNGA1, CNGB1, EYS, TOPORS, CERKL, KIAA1549, GNPTG, CYP4V2, CRB1, CRX, FLVCR1, FAM161A, ZNF513, C8orf37, SNRNP200, ECM1, PRCD, ABCA4, PCARE, FSCN2, GUCA1B, IDH3B, IMPDH1, LRAT, MAK, MERTK, NEK2, NR2E3, NRL, PDE6A, PDE6B, PDE6G, PROM1, BBS1, RBP3, RBP4, PRPH2, RGR Specificity 2 % Genes 100 %
Retinitis pigmentosa, AR and X-linked (NGS panel for 53 genes). By CGC Genetics (Portugal). RHO, RLBP1, RP1, RP2, RPE65, RPGR, SAG, TUB, TULP1, USH2A, BEST1, ADGRA3, RP1L1, ARL2BP, DHX38, NMNAT1, RDH11, IMPG2, RDH12, TTC8 , (...) View the complete list with 33 more genes Panel complete gene list RHO, RLBP1, RP1, RP2, RPE65, RPGR, SAG, TUB, TULP1, USH2A, BEST1, ADGRA3, RP1L1, ARL2BP, DHX38, NMNAT1, RDH11, IMPG2, RDH12, TTC8, SPATA7, DHDDS, CNGA1, CNGB1, EYS, CERKL, KIAA1549, GNPTG, CYP4V2, CRB1, FLVCR1, FAM161A, ZNF513, C8orf37, EMC1, PRCD, ABCA4, PCARE, IDH3B, LRAT, MAK, MERTK, NEK2, NR2E3, NRL, PDE6A, PDE6B, PDE6G, PROM1, BBS1, RBP3, RBP4, RGR Specificity 2 % Genes 100 %

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Sources and references

You can check the following sources for additional information.

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