Nanophthalmos 2; Nno2

Clinical Features

Phenotypes and symptoms related to Nanophthalmos 2; Nno2

  • Microphthalmia
  • Glaucoma
  • Retinal detachment
  • Angle closure glaucoma

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.

Alternative names

Nanophthalmos 2; Nno2 Is also known as nanophthalmia 2, nanophthalmos, autosomal recessive.

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.

Nanophthalmos 2; Nno2 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
MitoMet®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 %
Macular Degeneration Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).

RPGR, TIMP3, BEST1, C1QTNF5, ELOVL4, RP1L1, CDH3, RAX2, IMPG2, HMCN1, CNGB3, CTNNA1, MFSD8, DRAM2, EFEMP1, ABCA4, FBLN5, FSCN2, GUCA1B, IMPG1 , (...)

View the complete list with 4 more genes
Specificity
5 %
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
3 %
Genes
100 %
Retinal degeneration late-onset, AD (sequence analysis of C1QTNF5 gene).

By CGC Genetics (Portugal).

C1QTNF5
Specificity
100 %
Genes
50 %
Stargardt disease and macular distrophy (NGS panel for 14 genes).

By CGC Genetics (Portugal).

RPGR, TIMP3, BEST1, C1QTNF5, ELOVL4, RP1L1, CDH3, RDH12, CNGB3, ABCA4, FSCN2, IMPG1, PROM1, PRPH2
Specificity
8 %
Genes
50 %
Autosomal Dominant Retinitis Pigmentosa Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

RHO, ROM1, RP1, RPE65, SEMA4A, BEST1, CA4, C1QTNF5, PRPF31, KLHL7, PRPF6, PRPF8, PRPF3, PITPNM3, EYS, TOPORS, CRB1, CRX, EMC1, SNRNP200 , (...)

View the complete list with 9 more genes
Specificity
4 %
Genes
50 %
Retinitis Pigmentosa (includes RPGR ORF15) Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

RHO, RLBP1, ROM1, RP1, RP2, RPE65, RPGR, SAG, SEMA4A, TULP1, USH2A, CLRN1, BEST1, ARL6, RPGRIP1, CA4, ADGRA3, CACNA1F, C1QTNF5, CDHR1 , (...)

View the complete list with 60 more genes
Specificity
3 %
Genes
100 %
Stargardt Disease (STGD) and Macular Dystrophies Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

RLBP1, RPGR, RS1, TIMP3, BEST1, RPGRIP1, C1QTNF5, ELOVL4, RP1L1, CDH3, IMPG2, RDH12, CNGB3, CERKL, CRB1, EFEMP1, ABCA4, FSCN2, GUCA1B, PROM1 , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
50 %

You can get up to 51 more panels with our dedicated tool

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Sources and references

You can check the following sources for additional information.

MESH OMIM Rare Disease Search Engine

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