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Hepatoerythropoietic porphyria

1 OMIM reference -
1 associated gene
4 signs/symptoms

PROTEIN INTERACTIONS: 1

Muscular dystrophy, Selcen type

1 OMIM reference -
1 associated gene
No signs/symptoms info

Hepatoerythropoietic porphyria

Muscular dystrophy, Selcen type

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	UROD	(0.63)	BAG3

Citations in the biomedical literature:

Hepatoerythropoietic porphyria		Muscular dystrophy, Selcen type
	Synonym(s): - HEP		Synonym(s): (no synonyms)

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare renal disease - Rare skin disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: D017121		External references: 1 OMIM reference - No MeSH references

Hepatoerythropoietic porphyria
	Very frequent - Autosomal dominant inheritance - Hemolytic anemia - Skin photosensitivity - Thin skin
Muscular dystrophy, Selcen type
(no data available)