deafness, cataract, impaired intellectual development, and polyneuropathy
MONDO:0859159Mondo
Findings
No curated finding names deafness, cataract, impaired intellectual development, and polyneuropathy 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
14 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.
- Developmental cataractHPOHP:0000519
- 3 of 3 reported patients
- Hearing impairmentHPOHP:0000365
- 3 of 3 reported patients · Congenital onset
- Malar flatteningHPOHP:0000272
- 3 of 3 reported patients
- Prominent supraorbital ridgesHPOHP:0000336
- 3 of 3 reported patients
- Subcutaneous calcificationHPOHP:0007618
- 3 of 3 reported patients
- Sunken cheeksHPOHP:0009938
- 3 of 3 reported patients
- Autistic behaviorHPOHP:0000729
- 2 of 3 reported patients
- PolyneuropathyHPOHP:0001271
- 2 of 3 reported patients
- Severe global developmental delayHPOHP:0011344
- 2 of 3 reported patients
- Short philtrumHPOHP:0000322
- 2 of 3 reported patients
- StrabismusHPOHP:0000486
- 2 of 3 reported patients
- Moderate global developmental delayHPOHP:0011343
- 1 of 3 reported patients
Show the remaining 2
- Round earHPOHP:0100830
- 1 of 3 reported patients
- SynophrysHPOHP:0000664
- 1 of 3 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.
- PSMC3HGNC:9549
- Moderate · PanelApp Australia · Autosomal recessive · 2025
- Limited · Ambry Genetics · Autosomal recessive · 2023
Where it sits
- A kind of