ZFIN Human Disease: Meier-Gorlin syndrome 5

OBO ID: DOID:0080516

OBO ID: DOID:0080516

Term Name:	Meier-Gorlin syndrome 5	Search Ontology:
Synonyms:
Definition:	A Meier-Gorlin syndrome that has_material_basis_in homozygous mutation in the CDC6 gene on chromosome 17q21. https://www.omim.org/entry/613805
References:	OMIM:613805
Ontology:	Human Disease ( DOID:0080516 )

Relationships

is a type of:	autosomal recessive disease Meier-Gorlin syndrome autosomal recessive disease Meier-Gorlin syndrome Show first 5 Terms

OTHER Meier-Gorlin syndrome 5 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CDC6	cdc6	?Meier-Gorlin syndrome 5	613805

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None