Summary Literature (0)

DOID:0050681 - Borjeson-Forssman-Lehmann syndrome

Disease Ontology Definition: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.

Synonyms: BFLS, BORJ, Borjeson syndrome, MRXSBFL, intellectual deficiency-epilepsy-endocrine disorders syndrome, mental retardation, epilepsy, and endocrine disorder, syndromic X-linked mental retardation Borjeson-Forssman-Lehmann type,

Echinobase Genes :


OMIM:

MIM:301900 - borjeson-forssman-lehmann syndrome; bfls

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee