atrophoderma vermiculata
MONDO:0008849Mondo
Findings
No curated finding names atrophoderma vermiculata yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
17 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.
- Abnormal cheek morphologyHPOHP:0004426
- Very frequent (80% to 99% of cases)
- Abnormal epidermal morphologyHPOHP:0011124
- Very frequent (80% to 99% of cases)
- Atrophic scarsHPOHP:0001075
- Very frequent (80% to 99% of cases)
- Hypoplastic pilosebaceous unitsHPOHP:0007515
- Very frequent (80% to 99% of cases)
- Skin pitHPOHP:0100276
- Very frequent (80% to 99% of cases)
- Abnormality of the chinHPOHP:0000306
- Frequent (30% to 79% of cases)
- Follicular hyperkeratosisHPOHP:0007502
- Frequent (30% to 79% of cases)
- Hyperkeratotic papuleHPOHP:0045059
- Frequent (30% to 79% of cases)
- Periauricular skin pitsHPOHP:0100277
- Frequent (30% to 79% of cases)
- Abnormal forehead morphologyHPOHP:0000290
- Occasional (5% to 29% of cases)
- Abnormality of the neckHPOHP:0000464
- Occasional (5% to 29% of cases)
- Atypical behaviorHPOHP:0000708
- Occasional (5% to 29% of cases)
Show the remaining 5
- ErythemaHPOHP:0010783
- Occasional (5% to 29% of cases)
- Heart blockHPOHP:0012722
- Occasional (5% to 29% of cases)
- NeurofibromaHPOHP:0001067
- Occasional (5% to 29% of cases)
- PainHPOHP:0012531
- Occasional (5% to 29% of cases)
- PruritusHPOHP:0000989
- Occasional (5% to 29% 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.
- LRP1HGNC:6692
- Supportive · Orphanet · Autosomal recessive · 2021
Where it sits
- A kind of
Other names
1 name
Resolves to: atrophoderma vermiculata
- Also called
- folliculitis ulerythematosa reticulate