Retinitis Pigmentosa 42; Rp42

Clinical Features

Phenotypes and symptoms related to Retinitis Pigmentosa 42; Rp42

  • Rod-cone dystrophy
  • Pallor
  • Retinal degeneration

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.


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Retinitis Pigmentosa 42; Rp42 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
100 %
KLHL7 Comprehensive - Sequence & Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories (United States).

KLHL7
Specificity
100 %
Genes
100 %
KLHL7 Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories (United States).

KLHL7
Specificity
100 %
Genes
100 %
KLHL7 Sequence Analysis.

By Baylor Miraca Genetics Laboratories (United States).

KLHL7
Specificity
100 %
Genes
100 %
KLHL7 Sequence Analysis (Prenatal Diagnosis).

By Baylor Miraca Genetics Laboratories (United States).

KLHL7
Specificity
100 %
Genes
100 %
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
100 %
KLHL7.

By Institute for Human Genetics University Clinic Freiburg (Germany).

KLHL7
Specificity
100 %
Genes
100 %
KLHL7.

By Institute for Human Genetics University Clinic Freiburg (Germany).

KLHL7
Specificity
100 %
Genes
100 %

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Sources and references

You can check the following sources for additional information.

OMIM MESH Genetic Syndrome Finder

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