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basal cell nevus syndrome
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
PTCH1
SUFU
GSTT1
NHLH2
PTCH2
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
cell fate specification
PID_HEDGEHOG_GLI_PATHWAY
ventral spinal cord development
dorsal/ventral pattern formation
neural tube closure
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Curated Studies
Most Correlated Studies
Ameloblastoma and keratocystic odontogenic tumor gene expression analysis
OMIM - Cancer
Mouse Phenotypes - Autosomal dominant hereditary disorder
OMIM - Malignant neoplasms
Fibroblast and Keratinocyte cells of Basal cell nevus syndrome patients treated with sirolimus
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Literature
Most Relevant Literature
Treatment of Gorlin syndrome (nevoid basal cell carcinoma syndrome) with methylaminolevulinate photo…
Unicystic ameloblastoma associated with the novel K729M PTCH1 mutation in a patient with nevoid basa…
Urticaria after methyl aminolevulinate photodynamic therapy in a patient with nevoid basal cell carc…
Expression of podoplanin in nevoid basal cell carcinoma syndrome-associated keratocystic odontogenic…
Heterozygous tandem duplication within the PTCH1 gene results in nevoid basal cell carcinoma syndrom…
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Clinical Trials
Most Relevant Clinical Trials
Study of BMS-833923 in Two Specific Patients With Basal Cell Nevus Syndrome
Topical Sirolimus in Patients With Basal Cell Nevus Syndrome and in Healthy Participants
Celecoxib in Preventing Basal Cell Carcinoma in Patients With Basal Cell Nevus Syndrome
Blue vs Red Light During Levulan Based Photodynamic Therapy in Patients With Basal Cell Nevus Syndro…
Topical Tazarotene in Treating Patients With Basal Cell Skin Cancer and Basal Cell Nevus Syndrome on…
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