{"query":"intellectual disability","kind":"text","recognisedAs":"Free text","results":[{"kind":"phenotype","id":"HP:0001249","route":"/phenotype/HP%3A0001249/","label":"Intellectual disability","description":"HP:0001249 · Human Phenotype Ontology"},{"kind":"disease","id":"MONDO:0001071","route":"/disease/MONDO%3A0001071/","label":"intellectual disability","description":"MONDO:0001071 · MONDO"},{"kind":"disease","id":"MONDO:0010306","route":"/disease/MONDO%3A0010306/","label":"X-linked intellectual disability, Cabezas type","description":"MONDO:0010306 · MONDO"},{"kind":"disease","id":"MONDO:0010574","route":"/disease/MONDO%3A0010574/","label":"syndromic X-linked intellectual disability 5","description":"MONDO:0010574 · MONDO"},{"kind":"disease","id":"MONDO:0019181","route":"/disease/MONDO%3A0019181/","label":"non-syndromic X-linked intellectual disability","description":"MONDO:0019181 · MONDO"},{"kind":"disease","id":"MONDO:0014855","route":"/disease/MONDO%3A0014855/","label":"intellectual disability, autosomal dominant 42","description":"MONDO:0014855 · MONDO"},{"kind":"disease","id":"MONDO:0014858","route":"/disease/MONDO%3A0014858/","label":"intellectual disability, autosomal dominant 43","description":"MONDO:0014858 · MONDO"},{"kind":"disease","id":"MONDO:0010277","route":"/disease/MONDO%3A0010277/","label":"syndromic X-linked intellectual disability Shashi type","description":"MONDO:0010277 · MONDO"},{"kind":"disease","id":"MONDO:0012960","route":"/disease/MONDO%3A0012960/","label":"intellectual disability, autosomal dominant 5","description":"MONDO:0012960 · MONDO"},{"kind":"disease","id":"MONDO:0010501","route":"/disease/MONDO%3A0010501/","label":"syndromic X-linked intellectual disability 34","description":"MONDO:0010501 · MONDO"},{"kind":"disease","id":"MONDO:0010402","route":"/disease/MONDO%3A0010402/","label":"syndromic X-linked intellectual disability 94","description":"MONDO:0010402 · MONDO"}]}