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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Galloway-Mowat syndrome 1  
Galloway-Mowat Syndrome 10  
A severe autosomal recessive disorder characterized by onset of symptoms soon after birth (progressive renal dysfunction with proteinuria associated with diffuse mesangial sclerosis). Caused by homozygous or compound heterozygous mutation in the YRDC gene on chromosome 1p34.
Galloway-Mowat syndrome 2  
Galloway-Mowat syndrome 3  
Galloway-Mowat syndrome 4  
Galloway-Mowat syndrome 5  
Galloway-Mowat Syndrome 6  
Galloway-Mowat Syndrome 7  
Galloway-Mowat Syndrome 8  
Galloway-Mowat Syndrome 9  

Synonyms
Exact Synonyms: GAMOS10;  YRDC-RELATED CONDITION
Primary IDs: MIM:619609
Definition Sources: MIM:619609

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