neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities
MONDO:0032790Mondo
Findings
No curated finding names neurodevelopmental disorder with coarse facies and mild distal skeletal 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
- Infantile onset · Neonatal onset
HPO, annotations 2026-09-02
Features
230 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.
- 2-4 toe syndactylyHPOHP:0010714
- 1 of 1 reported patient
- Accommodative esotropiaHPOHP:0020046
- 1 of 1 reported patient
- Adrenal insufficiencyHPOHP:0000846
- 1 of 1 reported patient
- Aggressive behaviorHPOHP:0000718
- 9 of 9 reported patients
- AgitationHPOHP:0000713
- 1 of 1 reported patient
- AllergyHPOHP:0012393
- 1 of 1 reported patient
- AlopeciaHPOHP:0001596
- 1 of 1 reported patient
- AngerHPOHP:0031473
- 1 of 1 reported patient
- Anteverted naresHPOHP:0000463
- 4 of 4 reported patients
- AnxietyHPOHP:0000739
- 7 of 7 reported patients
- ApraxiaHPOHP:0002186
- 1 of 1 reported patient
- AspirationHPOHP:0002835
- 1 of 1 reported patient
Show the remaining 218
- AsthmaHPOHP:0002099
- 2 of 2 reported patients
- AstigmatismHPOHP:0000483
- 3 of 3 reported patients
- AtaxiaHPOHP:0001251
- 1 of 1 reported patient
- Attention deficit hyperactivity disorderHPOHP:0007018
- 20 of 20 reported patients
- AutismHPOHP:0000717
- 2 of 2 reported patients
- Axial hypotoniaHPOHP:0008936
- 1 of 1 reported patient
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.
- KDM6BHGNC:29012
- Strong · Ambry Genetics · Autosomal dominant · 2019
- Strong · Illumina · Autosomal dominant · 2020
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2023
- Strong · G2P · Autosomal dominant · 2025
- Strong · PanelApp Australia · Autosomal dominant · 2025