neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities
MONDO:0030866Mondo
Findings
No curated finding names neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities 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 · Neonatal onset
HPO, annotations 2026-09-02
Features
38 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.
- Delayed ability to walkHPOHP:0031936
- 5 of 5 reported patients
- Growth delayHPOHP:0001510
- 5 of 5 reported patients
- Hypoplasia of the corpus callosumHPOHP:0002079
- 5 of 5 reported patients
- MicrocephalyHPOHP:0000252
- 5 of 5 reported patients
- Hypertrophic cardiomyopathyHPOHP:0001639
- 4 of 5 reported patients
- Perisylvian polymicrogyriaHPOHP:0012650
- 4 of 5 reported patients
- Attention deficit hyperactivity disorderHPOHP:0007018
- 3 of 4 reported patients
- DysmetriaHPOHP:0001310
- 3 of 4 reported patients
- Severe intellectual disabilityHPOHP:0010864
- 2 of 3 reported patients
- 2-3 toe syndactylyHPOHP:0004691
- 3 of 5 reported patients
- Highly arched eyebrowHPOHP:0002553
- 3 of 5 reported patients
- Proximal placement of thumbHPOHP:0009623
- 3 of 5 reported patients
Show the remaining 26
- Spastic gaitHPOHP:0002064
- 2 of 4 reported patients
- Babinski signHPOHP:0003487
- 2 of 5 reported patients
- Conjunctival hyperemiaHPOHP:0030953
- 2 of 5 reported patients
- DroolingHPOHP:0002307
- 2 of 5 reported patients
- ScoliosisHPOHP:0002650
- 2 of 5 reported patients
- Slow saccadic eye movementsHPOHP:0000514
- 2 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.
- SHMT2HGNC:10852
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2022
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Strong · G2P · Autosomal recessive · 2020
- Limited · ClinGen · Autosomal recessive · 2024
Where it sits
Other names
1 name
Resolves to: neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities
- Also called
- NEDCASB