autosomal recessive cerebral atrophy
MONDO:0018218Mondo
Findings
No curated finding names autosomal recessive cerebral atrophy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
1 feature
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, hp/releases/2026-09-01.
- Cerebral atrophyMondoHP:0002059
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.
- TMPRSS4HGNC:11878
- Supportive · Orphanet · Autosomal recessive · 2021