keratoderma-ichthyosis-deafness syndrome, autosomal recessive
MONDO:0859278Mondo
Findings
No curated finding names keratoderma-ichthyosis-deafness syndrome, autosomal recessive 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 · Infantile onset
HPO, annotations 2026-09-02
Features
6 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.
- Congenital palmoplantar hyperkeratosisHPOHP:0007545
- 3 of 3 reported patients
- IchthyosisHPOHP:0008064
- 3 of 3 reported patients
- Sensorineural hearing impairmentHPOHP:0000407
- 3 of 3 reported patients
- Global developmental delayHPOHP:0001263
- 2 of 3 reported patients
- Autoamputation of digitsHPOHP:0007460
- 1 of 3 reported patients
- Talipes equinovarusHPOHP:0001762
- 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.
- VPS33BHGNC:12712
- Moderate · G2P · Autosomal recessive · 2025
Where it sits
- A kind of