neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities
MONDO:0859297Mondo
Findings
No curated finding names neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Congenital onset
HPO, annotations 2026-09-02
Features
47 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.
- BrachydactylyHPOHP:0001156
- 4 of 4 reported patients
- Clinodactyly of the 5th fingerHPOHP:0004209
- 4 of 4 reported patients
- Feeding difficultiesHPOHP:0011968
- 4 of 4 reported patients
- Global developmental delayHPOHP:0001263
- 5 of 5 reported patients
- Short distal phalanx of the 5th fingerHPOHP:0004227
- 4 of 4 reported patients
- BrachycephalyHPOHP:0000248
- 3 of 4 reported patients
- Broad halluxHPOHP:0010055
- 3 of 4 reported patients
- Broad thumbHPOHP:0011304
- 3 of 4 reported patients
- HirsutismHPOHP:0001007
- 3 of 4 reported patients
- MicrognathiaHPOHP:0000347
- 3 of 4 reported patients
- Motor stereotypyHPOHP:0000733
- 3 of 4 reported patients
- Pes valgusHPOHP:0008081
- 3 of 4 reported patients
Show the remaining 35
- Secondary microcephalyHPOHP:0005484
- 3 of 4 reported patients
- Short footHPOHP:0001773
- 3 of 4 reported patients
- Short palmHPOHP:0004279
- 3 of 4 reported patients
- StrabismusHPOHP:0000486
- 3 of 4 reported patients
- Upslanted palpebral fissureHPOHP:0000582
- 3 of 4 reported patients
- Cerebellar vermis hypoplasiaHPOHP:0001320
- 3 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.
- HNRNPRHGNC:5047
- Definitive · G2P · Autosomal dominant · 2025
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2023
- Strong · PanelApp Australia · Autosomal dominant · 2025