ODCs

Cytoscape Web

Click node...

Marie Unna hereditary hypotrichosis

2 OMIM references -
2 associated genes
6 signs/symptoms

COMMON GENES: 1
COMMON SIGNS: 3

Alopecia universalis

3 OMIM references -
1 associated gene
6 signs/symptoms

Marie Unna hereditary hypotrichosis

Alopecia universalis

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


COMMON GENES	HR

Citations in the biomedical literature:

Marie Unna hereditary hypotrichosis		Alopecia universalis
	Synonym(s): - Hypotrichosis, Marie Unna type - MUHH - Marie Unna congenital hypotrichosis		Synonym(s): (no synonyms)

	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: 3 OMIM references - 1 MeSH reference: C537055


COMMON SIGNS	- Absent / decreased / thin eyebrows - Alopecia - Hypotrichosis / atrichia / atrichiasis / scalp hairlessness

Marie Unna hereditary hypotrichosis		Alopecia universalis
	Very frequent - Anomalies of eyelids, eyelashes and lacrimal system - Autosomal dominant inheritance - Coarse / thick hair		Very frequent - Absent / decreased lashes - Autosomal recessive inheritance - Decreased body hair / axillar / pubic hairlessness