spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant
MONDO:0032660Mondo
Findings
No curated finding names spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Third trimester onset · Second trimester onset
HPO, annotations 2026-09-02
Features
25 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.
- Multiple joint contracturesHPOHP:0002828
- 2 of 2 reported patients
- Talipes equinovarusHPOHP:0001762
- 2 of 2 reported patients
- Adducted thumbHPOHP:0001181
- 1 of 2 reported patients
- Arthrogryposis multiplex congenitaHPOHP:0002804
- 1 of 2 reported patients
- Central apneaHPOHP:0002871
- 1 of 2 reported patients
- Cerebellar hypoplasiaHPOHP:0001321
- 1 of 2 reported patients
- Cerebellar vermis hypoplasiaHPOHP:0001320
- 1 of 2 reported patients
- Decreased fetal movementHPOHP:0001558
- 1 of 2 reported patients
- Extra-axial cerebrospinal fluid accumulationHPOHP:0012510
- 1 of 2 reported patients
- Feeding difficultiesHPOHP:0011968
- 1 of 2 reported patients
- Femur fractureHPOHP:0031846
- 1 of 2 reported patients
- Hand clenchingHPOHP:0001188
- 1 of 2 reported patients
Show the remaining 13
- Hip dislocationHPOHP:0002827
- 1 of 2 reported patients
- Hypoplasia of the corpus callosumHPOHP:0002079
- 1 of 2 reported patients
- Lateral ventricle dilatationHPOHP:0006956
- 1 of 2 reported patients
- MacrocephalyHPOHP:0000256
- 1 of 2 reported patients
- MicrognathiaHPOHP:0000347
- 1 of 2 reported patients
- Perisylvian polymicrogyriaHPOHP:0012650
- 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.
- BICD2HGNC:17208
- Strong · PanelApp Australia · Autosomal recessive · 2025
Where it sits
Other names
1 name
Resolves to: spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant
- Also called
- spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant