Osteopetrosis, Autosomal Recessive 2; Optb2

Clinical Features

Top most frequent phenotypes and symptoms related to Osteopetrosis, Autosomal Recessive 2; Optb2

  • Seizures
  • Short stature
  • Anemia
  • Visual impairment
  • Optic atrophy
  • Hydrocephalus
  • Blindness
  • Abnormality of the dentition
  • Thrombocytopenia
  • Mandibular prognathia

And another 18 symptoms. If you need more information about this disease we can help you.

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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

Osteopetrosis, Autosomal Recessive 2; Optb2 Is also known as osteopetrosis, osteoclast-poor, osteopetrosis, mild autosomal recessive form.

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.

Osteopetrosis, Autosomal Recessive 2; Optb2 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 %
TNFSF11 Sequence Analysis (Prenatal Diagnosis).

By Baylor Miraca Genetics Laboratories (United States).

TNFSF11
Specificity
100 %
Genes
100 %
TNFSF11 Sequence Analysis.

By Baylor Miraca Genetics Laboratories (United States).

TNFSF11
Specificity
100 %
Genes
100 %
TNFSF11 Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories (United States).

TNFSF11
Specificity
100 %
Genes
100 %
TNFSF11 Comprehensive - Sequence & Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories (United States).

TNFSF11
Specificity
100 %
Genes
100 %
TNFSF11. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).

TNFSF11
Specificity
100 %
Genes
100 %
Osteopetrosis via TNFSF11 Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

TNFSF11
Specificity
100 %
Genes
100 %
Skeletal Disorders and Joint Problems Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

RMRP, ROR2, RUNX2, SALL1, BMP1, BMP2, BMPR1B, SF3B4, SH3BP2, FBXW4, SHH, SHOX, SKI, SLCO2A1, SLC26A2, SMARCAL1, SMC1A, SOX9, SQSTM1, TBX15 , (...)

View the complete list with 236 more genes
Specificity
1 %
Genes
100 %

You can get up to 24 more panels with our dedicated tool

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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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