Retinitis Pigmentosa 36; Rp36
Clinical Features
Top most frequent phenotypes and symptoms related to Retinitis Pigmentosa 36; Rp36
- Cataract
- Edema
- Rod-cone dystrophy
- Pallor
- Scarring
- Optic disc pallor
- Macular degeneration
- Attenuation of retinal blood vessels
- Undetectable electroretinogram
- Macular edema
And another 4 symptoms. If you need more information about this disease we can help you.
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 36; Rp36 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
![]() By Baylor Miraca Genetics Laboratories (United States).
RGS9, RHO, GRK1, RLBP1, RNASEL, BCS1L, RP1, RP2, RP9, RPE65, RPGR, RPL35A, MRPL3, RPS14, RS1, SAG, SARDH, SCO2, SCP2, SDHB , (...)
View the complete list with 612 more genes
Specificity
1 %
Genes
50 % |
![]() By Baylor Miraca Genetics Laboratories (United States).
PRCD
Specificity
100 %
Genes
50 % |
![]() By Baylor Miraca Genetics Laboratories (United States).
PRCD
Specificity
100 %
Genes
50 % |
![]() By Baylor Miraca Genetics Laboratories (United States).
PRCD
Specificity
100 %
Genes
50 % |
![]() By Baylor Miraca Genetics Laboratories (United States).
PRCD
Specificity
100 %
Genes
50 % |
![]() By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).
RHO, RLBP1, ROM1, RP1, RP2, RP9, RPE65, RPGR, SAG, SEMA4A, SPP2, TULP1, USH2A, CLRN1, BEST1, ARL6, RPGRIP1, CA4, C1QTNF5, CDHR1 , (...)
View the complete list with 72 more genes
Specificity
2 %
Genes
50 % |
![]() By ARUP Laboratories, Molecular Genetics and Genomics (United States).
RHO, RLBP1, ROM1, RP1, RP2, RP9, RPE65, RPGR, SAG, SEMA4A, TULP1, USH2A, BEST1, RPGRIP1, CA4, CDHR1, PRPF31, KLHL7, PRPF8, PRPF3 , (...)
View the complete list with 33 more genes
Specificity
2 %
Genes
50 % |
![]() By CGC Genetics (Portugal).
PRCD
Specificity
100 %
Genes
50 % |
You can get up to 27 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
MESH OMIM Rare Disease Symptoms CheckerIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like ORTHOSTATIC INTOLERANCE CUSHING DISEASE DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL; DIAR1 MELANOSIS, NEUROCUTANEOUS; NCMS MENTAL RETARDATION, AUTOSOMAL DOMINANT 20; MRD20 ATTENTION DEFICIT-HYPERACTIVITY DISORDER; ADHD