Chondrocalcinosis 2
What's New
Last Posted: Mar 10, 2023
- Combined approach for finding susceptibility genes in DISH/chondrocalcinosis families: whole-genome-wide linkage and IBS/IBD studies.
Couto Ana Rita, et al. Human genome variation 2017 0 17041 - Genetic analysis of adults heterozygous for ALPL mutations.
Taillandier Agnès, et al. Journal of bone and mineral metabolism 2017 0 (6) 723-733 - Epidemiological, Clinical and Genetic Study of Hypophosphatasia in A Spanish Population: Identification of Two Novel Mutations in The Alpl Gene.
García-Fontana Cristina, et al. Scientific reports 2019 0 (1) 9569 - Calcium pyrophosphate crystal deposition in a cohort of 57 patients with Gitelman syndrome.
Chotard Emilie, et al. Rheumatology (Oxford, England) 2021 0 (6) 2494-2503 - The association between ANKH promoter polymorphism and chondrocalcinosis is independent of age and osteoarthritis: results of a case-control study.
Abhishek Abhishek, et al. Arthritis research & therapy 2014 0 (1) R25 - Chondrocalcinosis 1
From NCATS Genetic and Rare Diseases Information Center - Chondrocalcinosis 2
From NCATS Genetic and Rare Diseases Information Center - Chondrocalcinosis due to apatite crystal deposition
From NCATS Genetic and Rare Diseases Information Center - The hand arthropathy of hereditary hemochromatosis is strongly associated with iron overload.
Valenti Luca, et al. The Journal of rheumatology 2008 1 (1) 153-8 - Investigation of the role of ENPP1 and TNAP genes in chondrocalcinosis.
Zhang Y, et al. Rheumatology (Oxford, England) 2007 4 (4) 586-9
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Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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