An X-linked intellectual deficiency in which not enough information is known, reported or published to indicate whether a gene causes non-syndromic or syndromic presentations. [ https://clinicalgenome.org/affiliation/40006/ ]

Synonyms: X-linked intellectual disability

This is just here as a test because I lose it

Term information

Subsets

rare, inferred_rare, clingen

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/2670

creator

https://orcid.org/0000-0001-5208-3432

id

MONDO:0100284

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0100284

Term relations