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Hemochromatosis type 3
1 OMIM reference -
1 associated gene
3 connected diseases
No signs/symptoms info
Disease Type of connection
Porphyria cutanea tarda
Porphyria variegata
Congenital atransferrinemia
Synonym(s):
- TFR2-related hemochromatosis
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hepatic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
1 MeSH reference: C537248
Gene symbol UniProt reference OMIM reference
TFR2 Q9UP52604720
No signs/symptoms info available.