syndromic X-linked intellectual disability Raymond type
MONDO:0010427Mondo
Findings
No curated finding names syndromic X-linked intellectual disability Raymond type yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A syndromic X-linked intellectual disability characterized by intellectual disability and marfanoid habitus that has material basis in mutation in the ZDHHC9 gene on chromosome Xq26.1.
Definition from the Mondo Disease Ontology (MONDO:0010427), read 2026-09-29. CC BY 4.0.
Genes
1 gene
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.
- ZDHHC9HGNC:18475
- Definitive · ClinGen · X-linked · 2020
- Definitive · G2P · X-linked · 2025
- Strong · Labcorp Genetics (formerly Invitae) · X-linked · 2022
- Strong · PanelApp Australia · X-linked · 2025
Where it sits
Other names
2 names
Resolves to: syndromic X-linked intellectual disability Raymond type
- Also called
- intellectual disability, X-linked syndromic, Raymond typeMRXSR