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Marie Unna hereditary hypotrichosis

2 OMIM references -
2 associated genes
6 signs/symptoms

COMMON GENES: 1

Atrichia with papular lesions

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

Marie Unna hereditary hypotrichosis

Atrichia with papular lesions

EPS8L3	(UniProt - OMIM)		HR	(UniProt - OMIM)
HR	(UniProt - OMIM)


COMMON GENES	HR

Citations in the biomedical literature:

Marie Unna hereditary hypotrichosis		Atrichia with papular lesions
	Synonym(s): - Hypotrichosis, Marie Unna type - MUHH - Marie Unna congenital hypotrichosis		Synonym(s): - Papular atrichia

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the skin and subcutaneous tissue -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 2 OMIM references - 1 MeSH reference: C535912		External references: 1 OMIM reference - No MeSH references

Marie Unna hereditary hypotrichosis
	Very frequent - Absent / decreased / thin eyebrows - Alopecia - Anomalies of eyelids, eyelashes and lacrimal system - Autosomal dominant inheritance - Coarse / thick hair - Hypotrichosis / atrichia / atrichiasis / scalp hairlessness
Atrichia with papular lesions
(no data available)