neurodevelopmental disorder with relative macrocephaly and with or without cardiac or endocrine anomalies
MONDO:0032943Mondo
Findings
No curated finding names neurodevelopmental disorder with relative macrocephaly and with or without cardiac or endocrine anomalies yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
44 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 speech and language developmentHPOHP:0000750
- 4 of 4 reported patients
- Intellectual disabilityHPOHP:0001249
- 2 of 2 reported patients
- Motor delayHPOHP:0001270
- 5 of 5 reported patients
- HypertelorismHPOHP:0000316
- 4 of 5 reported patients
- Large foreheadHPOHP:0002003
- 3 of 5 reported patients
- Low-set earsHPOHP:0000369
- 3 of 5 reported patients
- Sleep apneaHPOHP:0010535
- 3 of 5 reported patients
- SeizureHPOHP:0001250
- 2 of 4 reported patients
- Bulbous noseHPOHP:0000414
- 2 of 5 reported patients
- Delayed ability to walkHPOHP:0031936
- 2 of 5 reported patients
- Feeding difficulties in infancyHPOHP:0008872
- 2 of 5 reported patients · Neonatal onset
- Gastroesophageal refluxHPOHP:0002020
- 2 of 5 reported patients
Show the remaining 32
- HypothyroidismHPOHP:0000821
- 2 of 5 reported patients
- MicrotiaHPOHP:0008551
- 2 of 5 reported patients
- Neonatal hypotoniaHPOHP:0001319
- 2 of 5 reported patients · Neonatal onset
- Pointed chinHPOHP:0000307
- 2 of 5 reported patients
- Prominent nasal bridgeHPOHP:0000426
- 2 of 5 reported patients
- Sparse eyebrowHPOHP:0045075
- 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.
- SPOPHGNC:11254
- Definitive · ClinGen · Autosomal dominant · 2025
- Strong · G2P · Autosomal dominant · 2025
Where it sits
Other names
1 name
Resolves to: neurodevelopmental disorder with relative macrocephaly and with or without cardiac or endocrine anomalies
- Also called
- nabais sa-de vries syndrome, type 2