intellectual disability, autosomal recessive 58
Findings
No curated finding names intellectual disability, autosomal recessive 58 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the ELP2 gene.
Definition from the Mondo Disease Ontology (MONDO:0014996), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Congenital onset · Infantile onset · Progressive
HPO, annotations 2026-09-02
Features
14 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.
- Absent speechHPOHP:0001344
- 2 of 2 reported patients
- Aggressive behaviorHPOHP:0000718
- 2 of 2 reported patients
- Axial hypotoniaHPOHP:0008936
- 2 of 2 reported patients
- ChoreoathetosisHPOHP:0001266
- 2 of 2 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 2 of 2 reported patients
- Global developmental delayHPOHP:0001263
- 2 of 2 reported patients
- HyperreflexiaHPOHP:0001347
Show the remaining 2
- Spastic diplegiaHPOHP:0001264
- 2 of 2 reported patients
- Short statureHPOHP:0004322
- 1 of 2 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.
- ELP2HGNC:18248
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2022
- Strong · G2P · Autosomal recessive · 2026
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · Ambry Genetics · Autosomal recessive · 2018
Where it sits
Other names
7 names
Resolves to: intellectual disability, autosomal recessive 58
- Also called
- autosomal recessive non-syndromic intellectual disability caused by mutation in ELP2ELP2 autosomal recessive non-syndromic intellectual disabilityintellectual developmental disorder, autosomal recessive 58intellectual disability, autosomal recessive type 58mental retardation, autosomal recessive 58mental retardation, autosomal recessive type 58MRT58