bent bone dysplasia syndrome 2
MONDO:0859573Mondo
Findings
No curated finding names bent bone dysplasia syndrome 2 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Congenital onset
HPO, annotations 2026-09-02
Features
31 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.
- Arthrogryposis multiplex congenitaHPOHP:0002804
- 3 of 3 reported patients
- Decreased calvarial ossificationHPOHP:0005474
- 3 of 3 reported patients
- Hypoplastic acetabulaeHPOHP:0003274
- 3 of 3 reported patients
- Intrauterine growth retardationHPOHP:0001511
- 3 of 3 reported patients
- MicropenisHPOHP:0000054
- 1 of 1 reported patient
- OsteopeniaHPOHP:0000938
- 3 of 3 reported patients
- PlatyspondylyHPOHP:0000926
- 3 of 3 reported patients
- Shawl scrotumHPOHP:0000049
- 1 of 1 reported patient
- Short neckHPOHP:0000470
- 3 of 3 reported patients
- Short tibiaHPOHP:0005736
- 3 of 3 reported patients
- Talipes equinovarusHPOHP:0001762
- 3 of 3 reported patients
- Ulnar bowingHPOHP:0003031
- 3 of 3 reported patients
Show the remaining 19
- Ulnar deviation of the handHPOHP:0009487
- 3 of 3 reported patients
- Bowed humerusHPOHP:0003865
- 2 of 3 reported patients
- Coronal cleft vertebraeHPOHP:0003417
- 2 of 3 reported patients
- Depressed nasal bridgeHPOHP:0005280
- 2 of 3 reported patients
- Relative macrocephalyHPOHP:0004482
- 2 of 3 reported patients
- Short lower limbsHPOHP:0006385
- 2 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.
- LAMA5HGNC:6485
- Limited · LiferaOmics · Autosomal recessive · 2026