neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies
MONDO:0032888Mondo
Findings
No curated finding names neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies 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
28 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.
- Global developmental delayHPOHP:0001263
- 5 of 5 reported patients
- BlindnessHPOHP:0000618
- 2 of 5 reported patients
- PlagiocephalyHPOHP:0001357
- 2 of 5 reported patients
- PolymicrogyriaHPOHP:0002126
- 2 of 5 reported patients
- ScoliosisHPOHP:0002650
- 2 of 5 reported patients
- SeizureHPOHP:0001250
- 2 of 5 reported patients
- Anteverted naresHPOHP:0000463
- 1 of 5 reported patients
- Broad neckHPOHP:0000475
- 1 of 5 reported patients
- Cerebellar hypoplasiaHPOHP:0001321
- 1 of 5 reported patients
- Cervical platyspondylyHPOHP:0004558
- 1 of 5 reported patients
- ColpocephalyHPOHP:0030048
- 1 of 5 reported patients
- Delayed CNS myelinationHPOHP:0002188
- 1 of 5 reported patients
Show the remaining 16
- Downturned corners of mouthHPOHP:0002714
- 1 of 5 reported patients
- Facial asymmetryHPOHP:0000324
- 1 of 5 reported patients
- HypertelorismHPOHP:0000316
- 1 of 5 reported patients
- Infantile spasmsHPOHP:0012469
- 1 of 5 reported patients
- MacrodontiaHPOHP:0001572
- 1 of 5 reported patients
- MicrocephalyHPOHP:0000252
- 1 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.
- DHX37HGNC:17210
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2020
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Limited · Ambry Genetics · Autosomal recessive · 2023
- Limited · G2P · Autosomal recessive · 2025