OBO ID: DOID:0111574 |
Term Name: | autosomal recessive woolly hair 3 | Search Ontology: | |
---|---|---|---|
Synonyms: |
|
||
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 ) |
OTHER autosomal recessive woolly hair 3 PAGES
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
Your Input Welcome
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if
additional information is required.
Oops. Something went wrong. Please try again later.