neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities
MONDO:0957225Mondo
Findings
No curated finding names neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities 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
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.
- Global developmental delayHPOHP:0001263
- 3 of 3 reported patients
- Hearing impairmentHPOHP:0000365
- 3 of 3 reported patients
- Limb joint contractureHPOHP:0003121
- 4 of 4 reported patients
- Myoclonic seizureHPOHP:0032794
- 4 of 4 reported patients · Neonatal onset
- Respiratory failureHPOHP:0002878
- 6 of 6 reported patients
- CryptorchidismHPOHP:0000028
- 3 of 4 reported patients
- Brain atrophyHPOHP:0012444
- 4 of 7 reported patients
- DysgyriaHPOHP:0032398
- 4 of 7 reported patients
- Limb hypertoniaHPOHP:0002509
- 4 of 7 reported patients
- Axial hypotoniaHPOHP:0008936
- 3 of 7 reported patients
- Cerebellar atrophyHPOHP:0001272
- 3 of 7 reported patients
- Exaggerated startle responseHPOHP:0002267
- 3 of 7 reported patients
Show the remaining 13
- Intrauterine growth retardationHPOHP:0001511
- 3 of 7 reported patients
- NystagmusHPOHP:0000639
- 2 of 5 reported patients
- Atrial septal defectHPOHP:0001631
- 2 of 6 reported patients
- CataractHPOHP:0000518
- 1 of 5 reported patients
- StrabismusHPOHP:0000486
- 1 of 5 reported patients
- HydronephrosisHPOHP:0000126
- 1 of 6 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.
- MED11HGNC:32687
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · G2P · Autosomal recessive · 2022
- Limited · Ambry Genetics · Autosomal recessive · 2024
Where it sits
- A kind of