Search Ontology:
Human Disease

Galloway-Mowat syndrome 5

Term ID
DOID:0080247
Synonyms
Definition
A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the TPRKB gene on chromosome 2p13. https://pubmed.ncbi.nlm.nih.gov/28805828/
References
Ontology
Human Disease   ( DOID:0080247 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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