ZFIN Human Disease: Meier-Gorlin syndrome 8

OBO ID: DOID:0080255

Term Name:	Meier-Gorlin syndrome 8		Search Ontology:
Synonyms:
Definition:	A Meier-Gorlin syndrome that has_material_basis_in compound heterozygous mutation in the MCM5 gene on chromosome 22q12. https://www.omim.org/entry/617564
References:	OMIM:617564
Ontology:	Human Disease ( DOID:0080255 )

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 8 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MCM5	mcm5	?Meier-Gorlin syndrome 8	617564

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None