1. Ministry of Health
Website:https://www.moh.gov.jo
Partnership Focus:Collaboration with the Ministry of Health supports alignment of dermatogenetic research with national health priorities. This partnership facilitates access to population-level data, ethical and regulatory frameworks, and the integration of genetic findings into public health planning and policy development.
Joint Activities:
Support for population-based studies and registry-linked research
Policy-informed research on the burden of genetic and dermatologic diseases
Potential shared funding initiatives and contributions to national precision medicine strategies
Impact:Enhances the translation of research findings into public health policy and strengthens the national framework for precision dermatology.
2. Jordanian Cancer Registry
Website:http://www.jcr.gov.jo
Partnership Focus:Collaboration with the Jordanian Cancer Registry provides access to high-quality, population-based national cancer incidence data, with a specific emphasis on skin cancers and their epidemiologic trends. This partnership supports dermatologic oncology research, including genotype–phenotype correlation studies, and enables investigation of the burden, distribution, and demographic patterns of cutaneous malignancies in Jordan.
Registry-linked epidemiologic, molecular, and translational studies
Collaborative research on genetic susceptibility and potential epigenetic factors in skin cancers
Integration of registry data with clinical phenotypes and, where available, genetic profiles
Impact:Strengthens evidence-based dermatologic oncology research and enhances Jordan’s national contribution to skin cancer epidemiology and genetics.
3. DEBRA International (Epidermolysis Bullosa Research Association)
Website:https://www.debra-international.org/post/new-eb-patient-organization-in-jordan
Partnership Focus:Collaboration with DEBRA International supports clinical and genetic research on Epidermolysis Bullosa (EB), with an emphasis on identifying novel mutations, characterizing phenotypic variability, and developing context-appropriate care models tailored to local healthcare systems. This partnership facilitates alignment with international standards in the study and management of inherited skin fragility disorders.
Engagement with global EB registries and collaborative research networks
Participation in educational, advocacy, and capacity-building initiatives
Impact:Enhances diagnostic accuracy, promotes multidisciplinary care, and improves long-term outcomes for patients affected by inherited dermatologic conditions.