Overview
X-linked hereditary disease is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Research Evidence
Peer-reviewed studies linked via MeSH term "Genetic Diseases, X-Linked" from the MEDLINE/PubMed database.
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Cataract surgery in megalocornea: A qualitative and quantitative evaluation of published literature.
[object Object], [object Object], [object Object] et al. · Acta Ophthalmol · 2025
PMID: 40013468Meta-Analysis
Infections in VEXAS syndrome: a systematic review of the literature.
[object Object], [object Object] · Curr Res Transl Med · 2025
PMID: 40561878Meta-Analysis
Ocular Features of VEXAS Syndrome: A Systematic Review and Meta-analysis.
[object Object], [object Object], [object Object] et al. · Am J Ophthalmol · 2025
PMID: 40157447Meta-Analysis
The role ofFDG-PET imaging in VEXAS syndrome: a multicentric case series and a systematic review of the literature.
[object Object], [object Object], [object Object] et al. · Intern Emerg Med · 2024
Prenatal Ultrasonographic Features Associated With ARSL and X-Linked Chondrodysplasia Punctata 1 (CDPX1): Literature Review and Case Series.
[object Object], [object Object], [object Object] et al. · Prenat Diagn · 2024
PMID: 39313411Meta-Analysis
Shedding light on myopia by studying complete congenital stationary night blindness.
[object Object], [object Object], [object Object] et al. · Prog Retin Eye Res · 2023
PMID: 36669906Meta-Analysis
A Case Report of IPEX Syndrome with Neonatal Diabetes Mellitus and Congenital Hypothyroidism as the Initial Presentation, and a Systematic Review of neonatal IPEX.
[object Object], [object Object], [object Object] · J Clin Immunol · 2023
PMID: 36867340Meta-Analysis
Experimental and approved treatments for skin photosensitivity in individuals with erythropoietic protoporphyria or X-linked protoporphyria: A systematic review.
[object Object], [object Object], [object Object] et al. · Biomed Pharmacother · 2023
PMID: 36525819Meta-Analysis
Oral manifestations of multisystemic inflammatory syndrome in children (MIS-C) and Kawasaki disease associated to COVID-19: A systematic review.
[object Object], [object Object], [object Object] et al. · Spec Care Dentist · 2022
Systematic Review of Outcomes After Cochlear Implantation in Children With X-Linked Deafness-2.
[object Object], [object Object], [object Object] et al. · Otolaryngol Head Neck Surg · 2021
PMID: 32600118Meta-Analysis
Search all PubMed articles for X-linked hereditary disease
Research data from MEDLINE/PubMed
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Lissencephaly type 1 due to doublecortin gene mutation(child)
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Female restricted epilepsy with intellectual disability syndrome(child)
X-linked intellectual disability Turner type(child)
X-linked intellectual disability Wilson type(child)
Wilson Turner syndrome(child)
Ataxia with deafness and intellectual disability syndrome(child)
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome(child)
Quick Facts
- SNOMED CT
- 128430005
- UMLS CUI
- C1138434
- Fully Specified Name
- X-linked hereditary disease (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.