ZFIN Human Disease: autosomal recessive dyskeratosis congenita 2

OBO ID: DOID:0070017

OBO ID: DOID:0070017

Term Name:	autosomal recessive dyskeratosis congenita 2	Search Ontology:
Synonyms:	DKCB2
Definition:	A dyskeratosis congenita that has_material_basis_in an autosomal recessive mutation of the NOLA2 gene on chromosome 5q35.3. https://www.ncbi.nlm.nih.gov/pubmed/18523010
References:	OMIM:613987
Ontology:	Human Disease ( DOID:0070017 )

Relationships

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

OTHER autosomal recessive dyskeratosis congenita 2 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NHP2	nhp2	Dyskeratosis congenita, autosomal recessive 2	613987

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None