RMRP related disorders - The RMRP gene encodes an RNA component of an enzyme involved in the processing of mitochondrial RNA. Mutations in RMRP have been identified in three different disorders: Cartilage-hair hypoplasia or metaphyseal chondrodysplasia, McKusick type (CHH; MIM 250250), metaphyseal dysplasia without hypotrichosis (CHHV; MIM 250460) and anauxetic dysplasia (MIM 607095). All are autosomal recessive disorders.

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Tests Available

By gene: RMRP
Sanger Sequencing
Test Code: 1019
Deletion / Duplication
Test Code: 1893
NGS/Del Dup Comprehensive
Test Code: 1894

Test Details

Technical Information
Disease Groups: 
Skeletal Dysplasias
CPT Codes: 
81479 x 1
Turnaround Time: 
Typically 1 to 2 weeks from receipt of a sample in the laboratory. All cases involving ongoing pregnancies will be expedited.
Non-Prenatal Specimens: 
  1. Whole blood: purple-top (EDTA) tube, minimum of 3 ml
  2. Genomic DNA: a minimum of 3 µg (at a concentration of at least 30 ng/µl)
  3. Fibroblasts: 2 confluent T-25 flasks
  4. Saliva: only samples collected in Oragene DNA Self-Collection Kit or Oragene Saliva Collection Kit for Young Children are accepted
Prenatal Specimens: 
  1. Cultured cells: 2 confluent T-25 flasks derived from amnio or CVS samples
  2. Genomic DNA: a minimum of 3 µg (at a concentration of at least 30 ng/µl)

Ship all specimen types at room temperature by overnight courier. Do not freeze.

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