retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome

Findings

No curated finding names retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome 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

Infantile onset

HPO, annotations 2026-09-02

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.

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.

Where it sits

A kind of

• hereditary disease
• multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
• syndromic disease

Resolves to: retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome

Also called

retinitis pigmentosa-deafness-premature aging-short stature-facial dysmorphism syndromeshort stature, hearing loss, retinitis pigmentosa, and distinctive facies