Knobloch syndrome 2
MONDO:0100119Mondo
Findings
No curated finding names Knobloch syndrome 2 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
19 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.
- Abnormal pulmonary interstitial morphologyHPOHP:0006530
- 2 of 2 reported patients
- Enamel hypoplasiaHPOHP:0006297
- 2 of 2 reported patients
- High myopiaHPOHP:0011003
- 2 of 2 reported patients
- MicrognathiaHPOHP:0000347
- 2 of 2 reported patients
- Retinal detachmentHPOHP:0000541
- 2 of 2 reported patients
- VitreoretinopathyHPOHP:0007773
- 2 of 2 reported patients
- Anterior cortical cataractHPOHP:0007795
- 1 of 2 reported patients
- AutismHPOHP:0000717
- 1 of 2 reported patients
- Bronchial wall thickeningHPOHP:0033542
- 1 of 2 reported patients
- Chronic constipationHPOHP:0012450
- 1 of 2 reported patients
- EncephaloceleHPOHP:0002084
- 1 of 2 reported patients
- Global developmental delayHPOHP:0001263
- 1 of 2 reported patients
Show the remaining 7
- Intellectual disabilityHPOHP:0001249
- 1 of 2 reported patients
- Patent ductus arteriosusHPOHP:0001643
- 1 of 2 reported patients
- Pyloric stenosisHPOHP:0002021
- 1 of 2 reported patients
- Recurrent respiratory infectionsHPOHP:0002205
- 1 of 2 reported patients
- SeizureHPOHP:0001250
- 1 of 2 reported patients
- Single umbilical arteryHPOHP:0001195
- 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.
- PAK2HGNC:8591
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Moderate · Ambry Genetics · Autosomal dominant · 2024
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2022
Where it sits
- A kind of