X-linked intellectual disability

GPTKB entity

Predicate	Object
gptkbp:instanceOf	genetic disorder intellectual disability
gptkbp:affects	cognitive development learning ability
gptkbp:cause	gptkb:Lesch-Nyhan_syndrome gptkb:ATR-X_syndrome gptkb:Allan-Herndon-Dudley_syndrome gptkb:Coffin-Lowry_syndrome gptkb:Fragile_X_syndrome gptkb:Lujan-Fryns_syndrome gptkb:MECP2_duplication_syndrome gptkb:Opitz_G/BBB_syndrome gptkb:Snyder-Robinson_syndrome gptkb:Waisman_syndrome gptkb:X-linked_adrenoleukodystrophy gptkb:X-linked_creatine_transporter_deficiency gptkb:X-linked_hydrocephalus gptkb:X-linked_spastic_paraplegia gptkb:Hunter_syndrome gptkb:Rett_syndrome gptkb:X-linked_agammaglobulinemia gptkb:Christianson_syndrome
gptkbp:causedBy	mutation in genes on the X chromosome
gptkbp:diagnosedBy	clinical evaluation genetic testing
gptkbp:firstDescribed	19th century
https://www.w3.org/2000/01/rdf-schema#label	X-linked intellectual disability
gptkbp:inheritance	X-linked
gptkbp:MeSH_ID	D008607
gptkbp:OMIM	309500
gptkbp:prevalence	more common in males
gptkbp:symptom	delayed speech learning difficulties behavioral problems delayed motor skills
gptkbp:treatment	behavioral therapy special education occupational therapy speech therapy supportive therapy
gptkbp:bfsParent	gptkb:Xq28
gptkbp:bfsLayer	6