BaseSpace
Correlation
Engine-Public
Sign In
Register
Home
My Data
Bookmarks
Collaborations
Inbox
Import Your Data
QuickView
FAQ
What is QuickView?
What can my QuickView results tell me?
What are the sources for the General Info tab in QuickView?
More QuickView FAQs
Back to top
QuickView
Curated
Studies
Body
Atlas
Disease
Atlas
Pharmaco
Atlas
Knockdown
Atlas
Genetic
Markers
Pathway
Enrichment
Literature
Clinical
Trials
0
Meta-
Analysis
QuickView
Search sequence regions
(e.g.
Hematopoietic cell
,
Tamoxifen
,
rs2300478
,
ERBB2
,
cell-cell adhesion
,
Lung cancer
)
Organisms
Chromosomes
Start
Stop
Homo Sapiens
Mus Musculus
Rattus Norvegicus
C. Elegans
D. Melanogaster
Saccharomyces Cerevisiae
QuickView
Go back to main search
Bookmark
Forward
QuickView
for
lentiginosis
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
No genes found
No SNPs found
Explore Genetic Markers Results
Pathway Enrichment
Most Correlated Biogroups
No biogroups found
Explore Pathway Enrichment Results
Curated Studies
Most Correlated Studies
Mouse Phenotypes - Autosomal dominant hereditary disorder
OMIM - LEOPARD syndrome
OMIM - Congenital disorder
Explore Curated Studies Results
Literature
Most Relevant Literature
Odyssey toward an understanding of acquired postinflammatory lentiginosis.
Nevus Spilus, Partial Unilateral Lentiginosis, and Linear and Whorled Nevoid Hypermelanosis: A Compa…
Picosecond 755-nm alexandrite laser treatment for oral lentiginosis in Peutz-Jeghers disease.
Eruptive facial lentiginosis-like repigmentation in a patient with longstanding generalized vitiligo…
Eruptive acral lentiginosis following chemotherapy for acute lymphoblastic leukemia: A case series.
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
Primary Pigmented Nodular Adrenocortical Disease (PPNAD) and the CARNEY Complex (CNC)
Defining the Genetic Basis for the Development of Primary Pigmented Nodular Adrenocortical Disease (…
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ