blepharophimosis-impaired intellectual development syndrome
MONDO:0859139Mondo
Findings
No curated finding names blepharophimosis-impaired intellectual development syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
68 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.
- BlepharophimosisHPOHP:0000581
- 14 of 14 reported patients
- EpicanthusHPOHP:0000286
- 14 of 14 reported patients
- Global developmental delayHPOHP:0001263
- 14 of 14 reported patients
- Intellectual disabilityHPOHP:0001249
- 14 of 14 reported patients
- Thin upper lip vermilionHPOHP:0000219
- 12 of 14 reported patients
- Sparse eyebrowHPOHP:0045075
- 11 of 14 reported patients
- Sparse eyelashesHPOHP:0000653
- 11 of 14 reported patients
- HypotoniaHPOHP:0001252
- 9 of 12 reported patients
- Delayed ability to walkHPOHP:0031936
- 10 of 14 reported patients
- Highly arched eyebrowHPOHP:0002553
- 10 of 14 reported patients
- Narrow palpebral fissureHPOHP:0045025
- 10 of 14 reported patients
- Wide nasal bridgeHPOHP:0000431
- 10 of 14 reported patients
Show the remaining 56
- Delayed speech and language developmentHPOHP:0000750
- 9 of 13 reported patients
- Exaggerated cupid's bowHPOHP:0002263
- 8 of 14 reported patients
- HypertelorismHPOHP:0000316
- 8 of 14 reported patients
- Tapered fingerHPOHP:0001182
- 8 of 14 reported patients
- Frontal bossingHPOHP:0002007
- 7 of 14 reported patients
- Underdeveloped nasal alaeHPOHP:0000430
- 7 of 14 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.
- SMARCA2HGNC:11098
- Strong · PanelApp Australia · Autosomal dominant · 2025
Where it sits
- A kind of
Other names
1 name
Resolves to: blepharophimosis-impaired intellectual development syndrome
- Also called
- SMARCA2-related blepharophimosis-intellectual disability syndrome