ZFIN Human Disease: autosomal recessive dyskeratosis congenita 6

OBO ID: DOID:0070024

OBO ID: DOID:0070024

Term Name:	autosomal recessive dyskeratosis congenita 6	Search Ontology:
Synonyms:	DKCB6
Definition:	A dyskeratosis congenita that has_material_basis_in an autosomal recessive mutation of the PARN gene on chromosome 16p13.12. https://www.ncbi.nlm.nih.gov/pubmed/25893599
References:	OMIM:616353
Ontology:	Human Disease ( DOID:0070024 )

Relationships

is a type of:	autosomal recessive disease dyskeratosis congenita autosomal recessive disease dyskeratosis congenita Show first 5 Terms

OTHER autosomal recessive dyskeratosis congenita 6 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
PARN	parn	Dyskeratosis congenita, autosomal recessive 6	616353

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None