Term Name: Galloway-Mowat syndrome 10
Synonyms:
Definition: A Galloway-Mowat syndrome characterized by onset of symptoms soon after birth that has_material_basis_in homozygous or compound heterozygous mutation in the YRDC gene on chromosome 1p34.
Ontology: Human Disease [DOID:0061293]   ( DOID:0061293 )

Relationships
is a type of: autosomal recessive disease Galloway-Mowat syndrome