Overview
Arachnodactyly is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Research Evidence
Peer-reviewed studies linked via MeSH term "Arachnodactyly" from the MEDLINE/PubMed database.
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Association between phenotype and deletion size in 22q11.2 microdeletion syndrome: systematic review and meta-analysis.
[object Object], [object Object], [object Object] et al. · Orphanet J Rare Dis · 2019
Non-pharmacological treatment of psychiatric disorders in individuals with 22q11.2 deletion syndrome; a systematic review.
[object Object], [object Object], [object Object] · Am J Med Genet A · 2018
Exploring the Cognitive and Behavioral Aspects of Shprintzen-Goldberg Syndrome; a Novel Cohort and Literature Review.
[object Object], [object Object], [object Object] et al. · Clin Genet · 2025
PMID: 39600231Review
Heterogeneity, crosstalk, and targeting of cancer-associated fibroblasts in cholangiocarcinoma.
[object Object], [object Object], [object Object] et al. · Hepatology · 2024
PMID: 37018128Review
Identification of a novel variant of SCARF2 in a Jordanian family with a van den Ende-Gupta Syndrome and literature review.
[object Object], [object Object], [object Object] et al. · Clin Dysmorphol · 2022
PMID: 35256560Review
22q11.2 deletion syndrome and congenital heart disease.
[object Object] · Am J Med Genet C Semin Med Genet · 2020
PMID: 32049433Review
Role of fibrillin-2 in the control of TGF-β activation in tumor angiogenesis and connective tissue disorders.
[object Object], [object Object], [object Object] et al. · Biochim Biophys Acta Rev Cancer · 2020
PMID: 32119940Review
Shprintzen-Goldberg syndrome: a rare disorder.
[object Object], [object Object] · Pan Afr Med J · 2016
Marfan Syndrome and Related Disorders: 25 Years of Gene Discovery.
[object Object], [object Object], [object Object] et al. · Hum Mutat · 2016
PMID: 26919284Review
TGF-β signalopathies as a paradigm for translational medicine.
[object Object], [object Object], [object Object] et al. · Eur J Med Genet · 2015
PMID: 26598797Review
Search all PubMed articles for Arachnodactyly
Research data from MEDLINE/PubMed
Related Conditions
CCA - Congenital contractural arachnodactyly(child)
Cranio-facio-digito-genital syndrome(child)
Arachnodactyly with abnormal ossification and intellectual disability syndrome(child)
Arachnodactyly and intellectual disability with facial dysmorphism syndrome(child)
Congenital abnormal shape of digit(parent)
Congenital deformity(parent)
Quick Facts
- SNOMED CT
- 62250003
- UMLS CUI
- C0003706
- Fully Specified Name
- Arachnodactyly (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.