neurocardiofaciodigital syndrome
MONDO:0859247Mondo
Findings
No curated finding names neurocardiofaciodigital syndrome 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
HPO, annotations 2026-09-02
Features
32 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.
- Narrow palpebral fissureHPOHP:0045025
- 3 of 3 reported patients
- RetrognathiaHPOHP:0000278
- 3 of 3 reported patients
- Severe global developmental delayHPOHP:0011344
- 3 of 3 reported patients
- Thin vermilion borderHPOHP:0000233
- 3 of 3 reported patients
- Failure to thriveHPOHP:0001508
- 2 of 3 reported patients
- Hearing impairmentHPOHP:0000365
- 2 of 3 reported patients
- Hypoplasia of the corpus callosumHPOHP:0002079
- 2 of 3 reported patients
- MicrocephalyHPOHP:0000252
- 2 of 3 reported patients
- Narrow foreheadHPOHP:0000341
- 2 of 3 reported patients
- NystagmusHPOHP:0000639
- 2 of 3 reported patients
- Overhanging nasal tipHPOHP:0011833
- 2 of 3 reported patients
- PolydactylyHPOHP:0010442
- 2 of 3 reported patients
Show the remaining 20
- Prominent foreheadHPOHP:0011220
- 2 of 3 reported patients
- Short statureHPOHP:0004322
- 2 of 3 reported patients
- Sparse eyebrowHPOHP:0045075
- 2 of 3 reported patients
- Sparse hairHPOHP:0008070
- 2 of 3 reported patients
- SyndactylyHPOHP:0001159
- 2 of 3 reported patients
- Atrial septal defectHPOHP:0001631
- 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.
- MAPKAPK5HGNC:6889
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023
- Strong · G2P · Autosomal recessive · 2021
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Limited · Ambry Genetics · Autosomal recessive · 2022
Where it sits
- A kind of