Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 GeneticVariation disease CLINVAR CHIPS for genetic testing to improve a regional clinical genetic service. 25046119 2015
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 Biomarker disease BEFREE Gene products mutated in the inherited bone marrow failure syndromes dyskeratosis congenita (DC), cartilage-hair hypoplasia (CHH), Diamond-Blackfan anemia (DBA), and Shwachman-Diamond syndrome (SDS) are all predicted to be involved in different aspects of ribosome synthesis. 16507776 2006
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 GeneticVariation disease BEFREE Here we report the prenatal testing for CHH in three Finnish and one Australian family using three DNA markers closely linked to the CHH gene. 7784364 1995
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 Biomarker disease BEFREE Based on its chromosomal location, expression pattern, and protein function, we considered TLN as a candidate gene for cartilage-hair hypoplasia (CHH), an autosomal recessive metaphyseal chondrodysplasia, previously mapped to 9p13. 10610730 1999
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 GeneticVariation disease CLINVAR Cartilage-hair hypoplasia (CHH), or metaphyseal dysplasia, McKusick type, is an autosomal recessive disease with diverse clinical manifestations. 16832578 2006
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 Biomarker disease BEFREE The manifestations of cartilage-hair hypoplasia (CHH), a metaphyseal chondrodysplasia caused by RMRP mutations, include short stature, hypoplastic hair, immunodeficiency and increased risk of malignancies. 28094436 2017
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 GeneticVariation disease BEFREE Therefore, alterations RMRP-S1 and -S2, caused by point mutations in RMRP, are strongly implicated in the molecular mechanism of CHH. 24009312 2014
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 Biomarker disease BEFREE Mutations on RNase MRP RNA gene (RMRP) cause a recessively inherited developmental disorder, cartilage-hair hypoplasia (CHH). 17189938 2007
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 Biomarker disease BEFREE Mutations in RMRP primarily give rise to Cartilage Hair Hypoplasia (CHH), a highly diverse skeletal disorder which can be associated with severe immunodeficiency. 25663137 2015
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 GeneticVariation disease CLINVAR A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease. 27569544 2016
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 Biomarker disease BEFREE Mutations in this gene are causing the highly pleiotropic disease cartilage-hair hypoplasia (CHH). 21956908 2012
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 Biomarker disease BEFREE Mutations in its RNA component lead to several autosomal recessive skeletal dysplasias, including cartilage-hair hypoplasia (CHH). 21053045 2011
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 Biomarker disease BEFREE Cartilage-hair hypoplasia (CHH) is a rare chondrodysplasia, including disproportionate short stature, hypoplastic hair, immunodeficiency, and increased risk of malignancies. 29462708 2018
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 GeneticVariation disease BEFREE We report on a 12-year-old girl with a new mutation of the RMRP gene and a severe multisystemic CHH (hematological and pulmonary lesions, severe immune deficiency, arthritis, pancreatic insufficiency, malabsorption, chronic diarrhea) receiving parenteral nutrition who presented with acute symptomatic hypocalcemia and hypercalciuria associated with the presence of autoantibodies directed against the calcium-sensor receptor. 19626344 2009
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 Biomarker disease GENOMICS_ENGLAND We conclude that mutations in RMRP cause CHH by disrupting a function of RNase MRP RNA that affects multiple organ systems. 11207361 2001
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 GeneticVariation disease CLINVAR RNase MRP and disease. 21956908 2012
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 GeneticVariation disease BEFREE Recent studies of cartilage-hair hypoplasia (CHH), a form of short-limbed dwarfism, have shown that all affected individuals have a cellular proliferation defect that results in a cellular immunodeficiency. 6223049 1983
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 CausalMutation disease CLINVAR RMRP mutations in Japanese patients with cartilage-hair hypoplasia. 14608646 2003
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 Biomarker disease BEFREE Both patients also had cartilage-hair hypoplasia (CHH). 16630949 2006
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 Biomarker disease BEFREE MDWH is caused by <i>RMRP</i> mutations, but it is differentiated from the allelic condition cartilage-hair hypoplasia (CHH), which in addition to chondrodysplasia is characterised by thin hair, immunodeficiency and increased risk of malignancy. 31413121 2020
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 CausalMutation disease CLINVAR Cartilage hair hypoplasia mutations that lead to RMRP promoter inefficiency or RNA transcript instability. 17937437 2007
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 Biomarker disease BEFREE Cartilage-hair hypoplasia (CHH) is a rare autosomal recessive skeletal dysplasia characterized by short stature, sparse hair, and a variable degree of immunodeficiency. 9115626 1997
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 Biomarker disease BEFREE Cartilage-hair hypoplasia (CHH) is a rare autosomal recessive disease caused by mutations in the RMRP gene. 20375313 2010
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 Biomarker disease GENOMICS_ENGLAND Cartilage-hair hypoplasia--clinical manifestations in 108 Finnish patients. 8444246 1993
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.700 GeneticVariation disease CLINVAR RMRP mutations in Japanese patients with cartilage-hair hypoplasia. 14608646 2003