Search Ontology:
Human Disease

autosomal recessive woolly hair 3

Term ID
DOID:0111574
Synonyms
  • ARWH3
Definition
A familial woolly hair syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the KRT24 gene on chromosome 17q21.2. https://www.ncbi.nlm.nih.gov/pubmed/26160856
References
Ontology
Human Disease   ( DOID:0111574 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models