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ankyloblepharon
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
No genes found
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
No biogroups found
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Curated Studies
Most Correlated Studies
OMIM - CHAND syndrome
OMIM - Hay-Wells syndrome
Neonatal keratinocytes with ΔNp63α overexpression or p63 siRNA knockdown
Keratinocytes from iPSCs of ankyloblepharon ectodermal dysplasia patients with the TP63 mutation
OMIM - Congenital disorder
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Literature
Most Relevant Literature
Cleft Lip With Ankyloblepharon Filiforme Adnatum: A Case Report.
Ankyloblepharon Filiforme Adnatum in a 3-day-old Neonate: A Case Report.
Rare Association of Ankyloblepharon Filiforme Adnatum (AFA) with Cleft Palate - Case Report.
Simple surgical approach for treatment of ankyloblepharon filiforme adnatum: A case report.
Congenital ankyloblepharon in a newborn with an IRF6 mutation.
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Clinical Trials
Most Relevant Clinical Trials
Salivary Gland Transplantation in the Treatment of Dry Eye in Patients With Stevens-Johnson Syndrome…
Ability of a Molecule (Prima) to Restore Physiological Differentiation in Epithelium Expressing Gene…
Topical rVA576 for Treatment of Atopic Keratoconjunctivitis
Randomized Clinical Trial Comparing the Safety and Efficacy of Rituximab Versus Oral Cyclophosphamid…
Clinical Trial Evaluating Rituximab in Ocular Cicatricial Pemphigoid
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