intellectual disability, X-linked, syndromic, Houge type
MONDO:0030909Mondo
Findings
No curated finding names intellectual disability, X-linked, syndromic, Houge type yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- X-linked inheritance
- Onset and course
- Infantile onset · Juvenile onset · Childhood onset
HPO, annotations 2026-09-02
Features
41 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.
- Aggressive behaviorHPOHP:0000718
- 1 of 1 reported patient
- Attention deficit hyperactivity disorderHPOHP:0007018
- 4 of 4 reported patients
- Bilateral tonic-clonic seizureHPOHP:0002069
- 2 of 2 reported patients
- Bilateral tonic-clonic seizure with generalized onsetHPOHP:0025190
- 2 of 2 reported patients
- Chiari malformationHPOHP:0002308
- 1 of 1 reported patient
- Clonic seizureHPOHP:0020221
- 1 of 1 reported patient
- Delayed speech and language developmentHPOHP:0000750
- 8 of 8 reported patients
- Distal joint hypermobilityHPOHP:0020152
- 1 of 1 reported patient
- EEG abnormalityHPOHP:0002353
- 1 of 1 reported patient
- Focal impaired awareness seizureHPOHP:0002384
- 1 of 1 reported patient
- Focal-onset seizureHPOHP:0007359
- 2 of 2 reported patients
- Generalized non-motor (absence) seizureHPOHP:0002121
- 1 of 1 reported patient
Show the remaining 29
- Generalized-onset motor seizureHPOHP:0032677
- 2 of 2 reported patients
- Global developmental delayHPOHP:0001263
- 12 of 12 reported patients
- HemiparesisHPOHP:0001269
- 1 of 1 reported patient
- Horizontal nystagmusHPOHP:0000666
- 1 of 1 reported patient
- ImpulsivityHPOHP:0100710
- 1 of 1 reported patient
- Intellectual disabilityHPOHP:0001249
- 3 of 3 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.
- CNKSR2HGNC:19701
- Strong · Labcorp Genetics (formerly Invitae) · X-linked · 2021
- Strong · G2P · X-linked · 2015
Where it sits
Other names
1 name
Resolves to: intellectual disability, X-linked, syndromic, Houge type
- Also called
- intellectual developmental disorder, X-linked, syndromic, Houge type