ZFIN Human Disease: autosomal dominant woolly hair

OBO ID: DOID:0111573

Term Name:	autosomal dominant woolly hair		Search Ontology:
Synonyms:	ADWH
Definition:	A familial woolly hair syndrome that has_material_basis_in heterozygous mutation in the KRT74 gene on chromosome 12q13.13. https://www.ncbi.nlm.nih.gov/pubmed/20346438
References:	OMIM:194300 SNOMEDCT_US_2022_07_31:403794008
Ontology:	Human Disease ( DOID:0111573 )

Relationships

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

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Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
KRT74		Woolly hair, autosomal dominant

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None