Marie Unna hereditary hypotrichosis |
Atrichia with papular lesions |
EPS8L3 | HR | |||
HR |
COMMON GENES |
HR |
Citations in the biomedical literature:
Marie Unna hereditary hypotrichosis |
Atrichia with papular lesions |
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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 -
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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)
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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) |