neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities
MONDO:0859312Mondo
Findings
No curated finding names neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities 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
48 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
- 5 of 5 reported patients
- HypotoniaHPOHP:0001252
- 5 of 5 reported patients
- Intellectual disabilityHPOHP:0001249
- 5 of 5 reported patients
- Narrow palpebral fissureHPOHP:0045025
- 5 of 5 reported patients
- Postnatal growth retardationHPOHP:0008897
- 5 of 5 reported patients
- Short statureHPOHP:0004322
- 5 of 5 reported patients
- Long faceHPOHP:0000276
- 4 of 5 reported patients
- Secondary microcephalyHPOHP:0005484
- 4 of 5 reported patients
- Clinodactyly of the 4th toeHPOHP:0011918
- 3 of 5 reported patients
- Clinodactyly of the 5th toeHPOHP:0001864
- 3 of 5 reported patients
- Hypoplasia of the corpus callosumHPOHP:0002079
- 3 of 5 reported patients
- Medial flaring of the eyebrowHPOHP:0010747
- 3 of 5 reported patients
Show the remaining 36
- Motor delayHPOHP:0001270
- 3 of 5 reported patients
- Pointed chinHPOHP:0000307
- 3 of 5 reported patients
- Absent speechHPOHP:0001344
- 2 of 5 reported patients
- Bulbous noseHPOHP:0000414
- 2 of 5 reported patients
- Clinodactyly of the 5th fingerHPOHP:0004209
- 2 of 5 reported patients
- Feeding difficultiesHPOHP:0011968
- 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.
- FRA10AC1HGNC:1162
- Strong · G2P · Autosomal recessive · 2022
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · Ambry Genetics · Autosomal recessive · 2023