protoporphyria, erythropoietic, 2
MONDO:0060729Mondo
Findings
No curated finding names protoporphyria, erythropoietic, 2 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Infantile onset
HPO, annotations 2026-09-02
Features
3 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.
- Cutaneous photosensitivityHPOHP:0000992
- 3 of 3 reported patients
- Increased erythrocyte protoporphyrin concentrationHPOHP:0012187
- 3 of 3 reported patients
- Iron deficiency anemiaHPOHP:0001891
- 1 of 3 reported patients
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.
- CLPXHGNC:2088
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2021