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GTR Home > Conditions/Phenotypes > Alopecia universalis congenita

Alopecia universalis congenita

Synonyms
ATRICHIA, GENERALIZED
Modes of inheritance
Autosomal recessive inheritance (Orphanet)
Non-Mendelian inheritance (Orphanet)

Summary

Alopecia universalis congenita (ALUNC) is a severe autosomal recessive form of alopecia characterized by a complete absence of hair development affecting all scalp and body hair (Nothen et al., 1998). This rare disorder is clearly distinct from alopecia areata (AA1; 104000), which has an autoimmune basis with probable genetic predisposition. [from OMIM]

Available tests

13 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (13 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: ALUNC, AU, HSA277165, HYPT4, MUHH, MUHH1, HR
    Summary: HR lysine demethylase and nuclear receptor corepressor

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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