ODCs

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1 associated gene
No signs/symptoms info

COMMON GENES: 1

3 OMIM references -
1 associated gene
No signs/symptoms info

Familial progressive hyper- and hypopigmentation

Familial progressive hyperpigmentation

Citations in the biomedical literature:

Familial progressive hyper- and hypopigmentation		Familial progressive hyperpigmentation
	Synonym(s): - FPHH		Synonym(s): - Melanosis diffusa congenita - Melanosis universalis hereditaria - Universal melanosis

	Classification (Orphanet): - Rare genetic disease - Rare skin disease		Classification (Orphanet): - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Diseases of the skin and subcutaneous tissue -		Classification (ICD10): - Diseases of the skin and subcutaneous tissue -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 3 OMIM references - No MeSH references

No signs/symptoms info available.