ZFIN Human Disease: autosomal recessive dyskeratosis congenita 3

OBO ID: DOID:0070019

Term Name:	autosomal recessive dyskeratosis congenita 3		Search Ontology:
Synonyms:	DKCB3
Definition:	A dyskeratosis congenita that has_material_basis_in an autosomal recessive mutation of the WRAP53 gene on chromosome 17p13.1. https://www.ncbi.nlm.nih.gov/pubmed/21205863
References:	OMIM:613988
Ontology:	Human Disease ( DOID:0070019 )

Relationships

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

OTHER autosomal recessive dyskeratosis congenita 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
WRAP53	wrap53	Dyskeratosis congenita, autosomal recessive 3	613988

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None