Last Posted: Nov 29, 2019
- Association of IL-6 -174G?>?C and -572G?>?C Polymorphisms with Risk of Legg-Calve-Perthes Disease in Iranian Children.
Akbarian-Bafghi Mohammad Javad, et al. Fetal and pediatric pathology 2019 11 1-8
- Association of eNOS 27-bp VNTR, 894G>T and 786T>C polymorphisms with susceptibility to Legg-Calve-Perthes Disease in Iranian children.
Azarpira Mohammad Reza, et al. Journal of orthopaedics 0 0 (2) 137-140
- Association of MTHFR and TNF-a genes polymorphisms with susceptibility to Legg-Calve-Perthes disease in Iranian children: A case-control study.
Azarpira Mohammad Reza, et al. Journal of orthopaedics 2018 12 (4) 984-987
- Endothelial nitric oxide synthase gene polymorphism is associated with Legg-Calvé-Perthes disease.
Zhao Yulong, et al. Experimental and therapeutic medicine 2016 5 (5) 1913-1917
- Legg-Calve-Perthes disease
From NCATS Genetic and Rare Diseases Information Center
- Coagulation abnormalities in Legg-Calvé-Perthes disease.
Vosmaer A, et al. The Journal of bone and joint surgery. American volume 2010 1 (1) 121-8
- Incidence of thrombophilia in patients with Gaucher disease.
Elstein D, et al. American journal of medical genetics 2000 12 (5) 429-31
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
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Graves Disease
- Huntington Disease
- Myasthenia Gravis
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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