joint laxity, short stature, and myopia
MONDO:0060556Mondo
Findings
No curated finding names joint laxity, short stature, and myopia yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
16 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.
- High myopiaHPOHP:0011003
- 5 of 5 reported patients
- Joint hypermobilityHPOHP:0001382
- 5 of 5 reported patients
- Short statureHPOHP:0004322
- 5 of 5 reported patients
- Talipes equinovarusHPOHP:0001762
- 3 of 5 reported patients
- Chorioretinal colobomaHPOHP:0000567
- 2 of 5 reported patients
- Hearing impairmentHPOHP:0000365
- 2 of 5 reported patients
- Iris colobomaHPOHP:0000612
- 2 of 5 reported patients · Congenital onset
- Multiple joint dislocationHPOHP:0012095
- 2 of 5 reported patients
- Pectus carinatumHPOHP:0000768
- 2 of 5 reported patients
- Retinal detachmentHPOHP:0000541
- 2 of 5 reported patients
- Cervical kyphosisHPOHP:0002947
- 1 of 5 reported patients
- GlaucomaHPOHP:0000501
- 1 of 5 reported patients
Show the remaining 4
- Inguinal herniaHPOHP:0000023
- 1 of 5 reported patients
- KyphoscoliosisHPOHP:0002751
- 1 of 5 reported patients
- Umbilical herniaHPOHP:0001537
- 1 of 5 reported patients
- Intellectual disabilityHPOHP:0001249
- 0 of 5 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.
- GZF1HGNC:15808
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2020
- Strong · G2P · Autosomal recessive · 2022
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Supportive · Orphanet · Autosomal recessive · 2021