ZFIN Human Disease: Galloway-Mowat syndrome 4

OBO ID: DOID:0080246

OBO ID: DOID:0080246

Term Name:	Galloway-Mowat syndrome 4	Search Ontology:
Synonyms:
Definition:	A Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TP53RK gene on chromosome 20q13. https://pubmed.ncbi.nlm.nih.gov/28805828/
References:	OMIM:617730
Ontology:	Human Disease ( DOID:0080246 )

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 4 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TP53RK	tp53rk	Galloway-Mowat syndrome 4	617730

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None