ZFIN Human Disease: Galloway-Mowat syndrome 3

OBO ID: DOID:0080245

OBO ID: DOID:0080245

Term Name:	Galloway-Mowat syndrome 3	Search Ontology:
Synonyms:
Definition:	A Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the OSGEP gene on chromosome 14q11. https://pubmed.ncbi.nlm.nih.gov/28805828/
References:	OMIM:617729
Ontology:	Human Disease ( DOID:0080245 )

Relationships

is a type of:	autosomal recessive disease Galloway-Mowat syndrome autosomal recessive disease Galloway-Mowat syndrome Show first 5 Terms

OTHER Galloway-Mowat syndrome 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
OSGEP	osgep	Galloway-Mowat syndrome 3	617729

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None