Term Name: autosomal recessive woolly hair 3
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.
Ontology: Human Disease [DOID:0111574]   ( DOID:0111574 )

Relationships
is a type of: autosomal recessive disease familial woolly hair syndrome