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hypotrichosis
(phenotype)
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Genetic Markers
Most Correlated Genes
Most Correlated SNPs
SOX18
CDH3
EPS8L3
C3orf52
DSC3
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Pathway Enrichment
Most Correlated Biogroups
hair cycle process
hair cycle
molting cycle
GSE17974_IL4_AND_ANTI_IL12_VS_UNTREATED_12H_ACT_CD4_TCELL_DN
GSE11961_PLASMA_CELL_DAY7_VS_GERMINAL_CENTER_BCELL_DAY40_UP
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Curated Studies
Most Correlated Studies
Roberts syndrome fibroblasts with ESCO2 mutations treated with L-leucine
OMIM - Hair finding
OMIM - Skeletal dysplasia
OMIM - Congenital disorder
OMIM - Disorder of hair growth
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Literature
Most Relevant Literature
Non-syndromic hypotrichosis: A report of two novel variants in the LSS gene.
Successful treatment of hereditary hypotrichosis simplex by platelet rich plasma injection with topi…
A case of congenital cataracts with hypotrichosis caused by compound heterozygous variants in the LS…
A case of LSS-associated congenital nuclear cataract with hypotrichosis and literature review.
Increased Hemichannel Activity Displayed by a Connexin43 Mutation Causing a Familial Connexinopathy …
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Clinical Trials
Most Relevant Clinical Trials
Bimatoprost for the Treatment of Eyebrow Hypotrichosis
Bimatoprost in the Treatment of Eyelash Hypotrichosis
An Observational Study of Patients Treated With Bimatoprost 0.03% (LatisseĀ®) for Hypotrichosis of th…
Efficacy of Topical Gentamycin for Hereditary Hypotrichosis Simplex Caused by Nonsense Mutations in …
Latisse (Bimatoprost .03% Opthalmic Solution) for the Treatment of Hypotrichosis of the Eyebrows: La…
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