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
database
cross reference
- UMLS:C1136249 (MONDO:equivalentTo)
- MEDGEN:211749 (MONDO:equivalentTo)
Subsets
otar, clingen