hereditary acrokeratotic poikiloderma, Weary type
MONDO:0017365Mondo
Findings
No curated finding names hereditary acrokeratotic poikiloderma, Weary type yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
47 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 blistering of the skinHPOHP:0008066
- Very frequent (80% to 99% of cases)
- Dystrophic fingernailsHPOHP:0008391
- Very frequent (80% to 99% of cases)
- Dystrophic toenailHPOHP:0001810
- Very frequent (80% to 99% of cases)
- Eczematoid dermatitisHPOHP:0000964
- Very frequent (80% to 99% of cases)
- ErythemaHPOHP:0010783
- Very frequent (80% to 99% of cases)
- GingivitisHPOHP:0000230
- Very frequent (80% to 99% of cases)
- Hypopigmented skin patchesHPOHP:0001053
- Very frequent (80% to 99% of cases)
- IchthyosisHPOHP:0008064
- Very frequent (80% to 99% of cases)
- Irregular hyperpigmentationHPOHP:0007400
- Very frequent (80% to 99% of cases)
- Nail dystrophyHPOHP:0008404
- Very frequent (80% to 99% of cases)
- PapuleHPOHP:0200034
- Very frequent (80% to 99% of cases)
- Premature loss of primary teethHPOHP:0006323
- Very frequent (80% to 99% of cases)
Show the remaining 35
- PustuleHPOHP:0200039
- Very frequent (80% to 99% of cases)
- Telangiectasia of the skinHPOHP:0100585
- Very frequent (80% to 99% of cases)
- Thin skinHPOHP:0000963
- Very frequent (80% to 99% of cases)
- UrticariaHPOHP:0001025
- Very frequent (80% to 99% of cases)
- Abnormal pigmentation of the oral mucosaHPOHP:0100669
- Frequent (30% to 79% of cases)
- Abnormal preputium morphologyHPOHP:0100587
- Frequent (30% to 79% of cases)
Where it sits
- A kind of
Other names
1 name
Resolves to: hereditary acrokeratotic poikiloderma, Weary type
- Also called
- congenital poikiloderma with bullae, Weary type