Boudin-Mortier syndrome
MONDO:0859194Mondo
Findings
No curated finding names Boudin-Mortier syndrome 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
20 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.
- Pseudoepiphyses of the middle phalanges of the handHPOHP:0010264
- 4 of 4 reported patients
- Pseudoepiphyses of the proximal phalanges of the handHPOHP:0010275
- 4 of 4 reported patients
- Pseudoepiphysis of the 1st metacarpalHPOHP:0010022
- 4 of 4 reported patients
- Tall statureHPOHP:0000098
- 4 of 4 reported patients
- Joint hypermobilityHPOHP:0001382
- 3 of 4 reported patients
- Aortic root aneurysmHPOHP:0002616
- 2 of 4 reported patients
- Long fingersHPOHP:0100807
- 2 of 4 reported patients
- Long halluxHPOHP:0001847
- 2 of 4 reported patients
- ArachnodactylyHPOHP:0001166
- 1 of 4 reported patients
- ClinodactylyHPOHP:0030084
- 1 of 4 reported patients
- Elevated alkaline phosphatase of bone originHPOHP:0010639
- 1 of 4 reported patients
- Gait disturbanceHPOHP:0001288
- 1 of 4 reported patients
Show the remaining 8
- Long thumbHPOHP:0032524
- 1 of 4 reported patients
- Long toeHPOHP:0010511
- 1 of 4 reported patients
- Malar flatteningHPOHP:0000272
- 1 of 4 reported patients
- Mallet fingerHPOHP:0030771
- 1 of 4 reported patients
- Mitral valve prolapseHPOHP:0001634
- 1 of 4 reported patients
- MyopiaHPOHP:0000545
- 1 of 4 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.
- NPR3HGNC:7945
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2021
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Strong · G2P · Autosomal recessive · 2019
Where it sits
- A kind of