neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia
MONDO:0859137Mondo
Findings
No curated finding names neurodevelopmental disorder with spasticity, cataracts, and cerebellar 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
32 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
- 14 of 14 reported patients
- Intellectual disabilityHPOHP:0001249
- 14 of 14 reported patients
- HypotoniaHPOHP:0001252
- 14 of 15 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 13 of 15 reported patients
- DystoniaHPOHP:0001332
- 13 of 15 reported patients
- Motor delayHPOHP:0001270
- 13 of 15 reported patients
- SpasticityHPOHP:0001257
- 13 of 15 reported patients
- Cerebellar atrophyHPOHP:0001272
- 12 of 14 reported patients
- CataractHPOHP:0000518
- 10 of 15 reported patients
- SeizureHPOHP:0001250
- 9 of 15 reported patients
- Feeding difficultiesHPOHP:0011968
- 8 of 14 reported patients
- DroolingHPOHP:0002307
- 7 of 14 reported patients
Show the remaining 20
- Developmental regressionHPOHP:0002376
- 5 of 15 reported patients
- Cerebral atrophyHPOHP:0002059
- 4 of 14 reported patients
- MicrocephalyHPOHP:0000252
- 4 of 14 reported patients
- Long eyelashesHPOHP:0000527
- 3 of 14 reported patients
- Anteverted naresHPOHP:0000463
- 2 of 14 reported patients
- Frontal upsweep of hairHPOHP:0002236
- 2 of 14 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.
- MED27HGNC:2377
- Definitive · ClinGen · Autosomal recessive · 2025
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023
- Strong · G2P · Autosomal recessive · 2021
- Strong · PanelApp Australia · Autosomal recessive · 2025