X-linked intellectual disability
MONDO:0100284Mondo
Findings
No curated finding names X-linked intellectual disability yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
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.
Definition from the Mondo Disease Ontology (MONDO:0100284), read 2026-09-29. CC BY 4.0.
Genes
6 genes
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- HCFC1HGNC:4839
- Definitive · Illumina · X-linked · 2021
- Definitive · ClinGen · X-linked · 2021
- ARHGEF6HGNC:685
- Limited · Ambry Genetics · X-linked · 2024
- SMARCA1HGNC:11097
- Limited · ClinGen · X-linked · 2022
- MAGT1HGNC:28880
- Disputed Evidence · ClinGen · X-linked · 2023
- ZNF674HGNC:17625
- Disputed Evidence · ClinGen · X-linked · 2021
- ZNF81HGNC:13156
- Disputed Evidence · ClinGen · X-linked · 2021
- Disputed Evidence · PanelApp Australia · X-linked · 2025