familial Alzheimer-like prion disease
MONDO:0017233Mondo
Findings
No curated finding names familial Alzheimer-like prion disease yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
12 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.
- Abdominal symptomHPOHP:0011458
- Very frequent (80% to 99% of cases)
- AnxietyHPOHP:0000739
- Very frequent (80% to 99% of cases)
- Attention deficit hyperactivity disorderHPOHP:0007018
- Very frequent (80% to 99% of cases)
- Atypical behaviorHPOHP:0000708
- Very frequent (80% to 99% of cases)
- Cognitive impairmentHPOHP:0100543
- Very frequent (80% to 99% of cases)
- Deficit in phonologic short-term memoryHPOHP:0002549
- Very frequent (80% to 99% of cases)
- DepressionHPOHP:0000716
- Very frequent (80% to 99% of cases)
- Emotional labilityHPOHP:0000712
- Very frequent (80% to 99% of cases)
- Jaw painHPOHP:0040264
- Very frequent (80% to 99% of cases)
- Perseverative thoughtHPOHP:0030223
- Very frequent (80% to 99% of cases)
- Sleep disturbanceHPOHP:0002360
- Very frequent (80% to 99% of cases)
- Specific learning disabilityHPOHP:0001328
- Very frequent (80% to 99% of cases)
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.
- HGNC:9449HGNC:9449
- Supportive · Orphanet · Autosomal dominant · 2021