intellectual disability, X-linked 97
Findings
No curated finding names intellectual disability, X-linked 97 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the ZNF711 gene.
Definition from the Mondo Disease Ontology (MONDO:0010430), read 2026-09-29. CC BY 4.0.
- Inheritance
- X-linked inheritance
- Onset and course
- Childhood onset
HPO, annotations 2026-09-02
Features
11 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Intellectual disabilityHPOHP:0001249
- 11 of 11 reported patients
- Moderate intellectual disabilityHPOHP:0002342
- 11 of 11 reported patients · Male
- Delayed speech and language developmentHPOHP:0000750
- 10 of 11 reported patients
- Broad faceHPOHP:0000283
- 6 of 11 reported patients
- Long faceHPOHP:0000276
- 4 of 11 reported patients
- MacrotiaHPOHP:0000400
- 4 of 11 reported patients
- Motor delayHPO
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.
- ZNF711HGNC:13128
- Definitive · G2P · X-linked · 2025
- Strong · Ambry Genetics · X-linked · 2024
- Strong · Labcorp Genetics (formerly Invitae) · X-linked · 2022
- Strong · PanelApp Australia · X-linked · 2025
Where it sits
Other names
5 names
Resolves to: intellectual disability, X-linked 97
- Also called
- intellectual developmental disorder, X-linked 97intellectual disability, X-linked type 97mental retardation, X-linked type 97non-syndromic X-linked intellectual disability caused by mutation in ZNF711ZNF711 non-syndromic X-linked intellectual disability