borjeson-forssman-lehmann syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An X-linked disease that is characterized by intellectual disability, truncal obesity, seizures, hypogonadism, developmental delay, distinctive facial features, tapered fingers and short toes and has_material_basis_in X-linked recessive inheritance of mutations in the PHF6 gene. (Human Disease Ontology, DOID_0050681)
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Genes

10 genes co-occuring with the disease borjeson-forssman-lehmann syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PHF6 PHD finger protein 6 2.4837
SMARCE1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 1.3869
ARID1B AT rich interactive domain 1B (SWI1-like) 1.20266
ARID1A AT rich interactive domain 1A (SWI-like) 0.963728
BANF1 barrier to autointegration factor 1 0.939949
KLF10 Kruppel-like factor 10 0.798282
SMARCB1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 0.791721
SMARCA4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 0.783936
MECOM MDS1 and EVI1 complex locus 0.766351
SMARCA2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 0.756156