ZFIN Human Disease: autosomal recessive woolly hair 3

OBO ID: DOID:0111574

OBO ID: DOID:0111574

Term Name:	autosomal recessive woolly hair 3	Search Ontology:
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:	OMIM:616760
Ontology:	Human Disease ( DOID:0111574 )

Relationships

is a type of:	autosomal recessive disease familial woolly hair syndrome autosomal recessive disease familial woolly hair syndrome Show first 5 Terms

OTHER autosomal recessive woolly hair 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
KRT25		Woolly hair, autosomal recessive 3

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None