neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia
MONDO:0859361Mondo
Findings
No curated finding names neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia 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
25 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 CNS myelinationHPOHP:0002188
- 4 of 4 reported patients
- Global developmental delayHPOHP:0001263
- 4 of 4 reported patients
- Hypoplasia of the corpus callosumHPOHP:0002079
- 4 of 4 reported patients
- NeurodegenerationHPOHP:0002180
- 4 of 4 reported patients
- Recurrent respiratory infectionsHPOHP:0002205
- 4 of 4 reported patients
- Reduced bone mineral densityHPOHP:0004349
- 4 of 4 reported patients
- Decreased total leukocyte countHPOHP:0001882
- 3 of 4 reported patients
- Decreased total lymphocyte countHPOHP:0001888
- 3 of 4 reported patients
- HypotoniaHPOHP:0001252
- 3 of 4 reported patients · Infantile onset
- SeizureHPOHP:0001250
- 3 of 4 reported patients
- SplenomegalyHPOHP:0001744
- 3 of 4 reported patients · Infantile onset
- VentriculomegalyHPOHP:0002119
- 3 of 4 reported patients
Show the remaining 13
- Decreased circulating IgG concentrationHPOHP:0004315
- 2 of 4 reported patients
- HepatomegalyHPOHP:0002240
- 2 of 4 reported patients · Infantile onset
- Joint dislocationHPOHP:0001373
- 2 of 4 reported patients
- Joint hypermobilityHPOHP:0001382
- 2 of 4 reported patients
- Postnatal growth retardationHPOHP:0008897
- 2 of 4 reported patients
- Recurrent skin infectionsHPOHP:0001581
- 2 of 4 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.
- NAE1HGNC:621
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · G2P · Autosomal recessive · 2023
- Limited · Ambry Genetics · Autosomal recessive · 2023
- Limited · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023