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Ontology Browser

Term:
Galloway-Mowat Syndrome 6 (DOID:9000383)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1)
Parent Terms Term With Siblings Child Terms
Galloway-Mowat Syndrome 1  
Galloway-Mowat syndrome 2  
Galloway-Mowat syndrome 3  
Galloway-Mowat syndrome 4  
Galloway-Mowat syndrome 5  
Galloway-Mowat Syndrome 6  
Galloway-Mowat syndrome is a phenotypically heterogeneous disorder characterized by neurodevelopmental defects combined with renal-glomerular disease manifest as nephrotic syndrome and proteinuria. Most patients with Galloway-Mowat syndrome-6 (GAMOS6) also have growth deficiency with variable microcephaly, and the renal disease may be age-dependent. Additional variable endocrine abnormalities have also been reported. GAMOS6 is caused by homozygous or compound heterozygous mutation in the WDR4 gene on chromosome 21q22. (OMIM)
Galloway-Mowat Syndrome 7  
Galloway-Mowat Syndrome 8  

Synonyms
Exact Synonyms: GAMOS6
Primary IDs: OMIM:618347

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.