spastic paraparesis-cataracts-speech delay syndrome
MONDO:0036212Mondo
Findings
No curated finding names spastic paraparesis-cataracts-speech delay syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Infantile onset
HPO, annotations 2026-09-02
Features
13 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.
- CataractHPOHP:0000518
- 12 of 12 reported patients
- Delayed ability to walkHPOHP:0031936
- 12 of 12 reported patients
- Spastic paraparesisHPOHP:0002313
- 12 of 12 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 10 of 12 reported patients
- Axial hypotoniaHPOHP:0008936
- 6 of 12 reported patients
- Bilateral tonic-clonic seizureHPOHP:0002069
- 6 of 12 reported patients
- Chronic constipationHPOHP:0012450
- 5 of 12 reported patients
- DysarthriaHPOHP:0001260
- 3 of 12 reported patients
- Focal motor seizureHPOHP:0011153
- 2 of 12 reported patients
- Generalized non-motor (absence) seizureHPOHP:0002121
- 2 of 12 reported patients
- MacrocephalyHPOHP:0000256
- 2 of 12 reported patients
- Complex febrile seizureHPOHP:0011172
- 1 of 12 reported patients
Show the remaining 1
- Impaired executive functioningHPOHP:0033051
- 1 of 12 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.
- FAR1HGNC:26222
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2021
Where it sits
- A kind of
Other names
1 name
Resolves to: spastic paraparesis-cataracts-speech delay syndrome
- Also called
- Fatty acyl-CoA reductase 1 superactivity