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aplasia cutis congenita
(phenotype)
Summary
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Genetic Markers
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UBA2
BMS1
Acc
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
COLDREN_GEFITINIB_RESISTANCE_UP
Ubiquitin/SUMO-activating enzyme ubiquitin-like domain
SUMO-activating enzyme subunit 2, C-terminal domain
SUMO-activating enzyme subunit Uba2
Ribosome biogenesis protein Bms1, N-terminal
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OMIM - Multisystem Complex Disorders
OMIM - Aplasia cutis congenita
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Literature
Most Relevant Literature
A rare case of aplasia cutis congenita.
Epidemiology of aplasia cutis congenita: A population-based study in Europe.
A rare case of extensive aplasia cutis congenita: Our surgical approach.
Choroidal calcifications in two cases of aplasia cutis congenita and oculoectodermal syndrome.
Conservative Management of a Rare Entity-Aplasia Cutis Congenita: A Case Report.
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Clinical Trials
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Genetic and Functional Analysis of Aplasia Cutis Congenital (ACC)
Relevance of Trichoscopy in Differential Diagnosis of Focal Non-cicatricial Alopecia in Children
Pregnancy and Neonatal Follow-up of Ongoing Pregnancies Established in Clinical Trial P05690 (Care P…
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