intellectual disability, X-linked 104
Findings
No curated finding names intellectual disability, X-linked 104 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 FRMPD4 gene.
Definition from the Mondo Disease Ontology (MONDO:0010509), read 2026-09-29. CC BY 4.0.
- Inheritance
- X-linked recessive inheritance
- Onset and course
- Infantile onset
HPO, annotations 2026-09-02
Features
29 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.
- Delayed gross motor developmentHPOHP:0002194
- 6 of 6 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 10 of 10 reported patients
- Global developmental delayHPOHP:0001263
- 10 of 10 reported patients
- Intellectual disabilityHPOHP:0001249
- 10 of 10 reported patients
- HyperreflexiaHPOHP:0001347
- 3 of 4 reported patients
- Autistic behaviorHPOHP:0000729
- 4 of 7 reported patients
- AtaxiaHPO
Show the remaining 17
- Delayed ability to walkHPOHP:0031936
- 4 of 10 reported patients
- Absent speechHPOHP:0001344
- 3 of 10 reported patients
- SeizureHPOHP:0001250
- 3 of 10 reported patients
- High foreheadHPOHP:0000348
- 2 of 8 reported patients
- RetrognathiaHPOHP:0000278
- 2 of 8 reported patients
- NystagmusHPOHP:0000639
- 2 of 9 reported patients
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.
- FRMPD4HGNC:29007
- Strong · Ambry Genetics · X-linked · 2018
- Strong · Labcorp Genetics (formerly Invitae) · X-linked · 2023
- Strong · G2P · X-linked · 2025
- Strong · PanelApp Australia · X-linked · 2025
- Moderate · Illumina · X-linked · 2020
Where it sits
Other names
7 names
Resolves to: intellectual disability, X-linked 104
- Also called
- FRMPD4 non-syndromic X-linked intellectual disabilityintellectual developmental disorder, X-linked 104intellectual disability, X-linked type 104mental retardation, X-linked 104mental retardation, X-linked type 104MRX104non-syndromic X-linked intellectual disability caused by mutation in FRMPD4