neurodevelopmental disorder with microcephaly and structural brain anomalies
MONDO:0032779Mondo
Findings
No curated finding names neurodevelopmental disorder with microcephaly and structural brain 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
16 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.
- Aggressive behaviorHPOHP:0000718
- 3 of 3 reported patients
- Anteverted naresHPOHP:0000463
- 3 of 3 reported patients
- Attention deficit hyperactivity disorderHPOHP:0007018
- 3 of 3 reported patients
- Bulbous noseHPOHP:0000414
- 3 of 3 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 5 of 5 reported patients
- DysarthriaHPOHP:0001260
- 3 of 3 reported patients
- Global developmental delayHPOHP:0001263
- 5 of 5 reported patients
- MicrocephalyHPOHP:0000252
- 5 of 5 reported patients · Congenital onset
- Motor delayHPOHP:0001270
- 5 of 5 reported patients
- SeizureHPOHP:0001250
- 2 of 2 reported patients
- Severe intellectual disabilityHPOHP:0010864
- 5 of 5 reported patients
- Simplified gyral patternHPOHP:0009879
- 3 of 3 reported patients
Show the remaining 4
- Upslanted palpebral fissureHPOHP:0000582
- 3 of 3 reported patients
- Absent septum pellucidumHPOHP:0001331
- 1 of 3 reported patients
- Agenesis of corpus callosumHPOHP:0001274
- 1 of 3 reported patients
- Hypoplasia of the corpus callosumHPOHP:0002079
- 1 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.
- DYNC1I2HGNC:2964
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2019
- Strong · G2P · Autosomal recessive · 2019
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Limited · Ambry Genetics · Autosomal recessive · 2019