# syndromic X-linked intellectual disability Raymond type

> 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

**Wikidata**: [Q28065628](https://www.wikidata.org/wiki/Q28065628)  
**Source**: https://4ort.xyz/entity/syndromic-x-linked-intellectual-disability-raymond-type


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations in ZDHHC9, Which Encodes a Palmitoyltransferase of NRAS and HRAS, Cause X-Linked Mental Retardation Associated with a Marfanoid Habitus
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/2156b925-1ee6-4edb-a514-3650aa5b780e--2020-08-12T14:50:49)
6. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_2156b925-1ee6-4edb-a514-3650aa5b780e-2020-08-12T145049.185Z)
7. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_2156b925-1ee6-4edb-a514-3650aa5b780e-2020-05-19T160000.000Z)
8. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000188706/MONDO_0010427)
9. [Identifiers.org](https://registry.identifiers.org/registry/doid)