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.

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 36; Rp36 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
MitoMetĀ®Plus aCGH Analysis.

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 %
PRCD Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories (United States).

PRCD
Specificity
100 %
Genes
50 %
PRCD Comprehensive - Sequence & Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories (United States).

PRCD
Specificity
100 %
Genes
50 %
PRCD Sequence Analysis.

By Baylor Miraca Genetics Laboratories (United States).

PRCD
Specificity
100 %
Genes
50 %
PRCD Sequence Analysis (Prenatal Diagnosis).

By Baylor Miraca Genetics Laboratories (United States).

PRCD
Specificity
100 %
Genes
50 %
Retinitis Pigmentosa Panel.

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 %
Retinitis Pigmentosa/Leber Congenital Amaurosis Panel, Sequencing and Deletion/Duplication.

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 %
Retinitis pigmentosa 36 (sequence analysis of PRCD gene).

By CGC Genetics (Portugal).

PRCD
Specificity
100 %
Genes
50 %

You can get up to 27 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

MESH OMIM Rare Disease Symptoms Checker

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like ORTHOSTATIC INTOLERANCE MACROCEPHALY/AUTISM SYNDROME MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE); MTDPS4A FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB; ARCL1B MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3; MDDGC3