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Galloway-Mowat Syndrome 7 (DOID:9001199)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (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 7  
Galloway-Mowat syndrome-7 (GAMOS7) is an autosomal recessive disorder characterized by developmental delay, microcephaly, and early-onset nephrotic syndrome. GAMOS7 is caused by homozygous or compound heterozygous mutation in the NUP107 gene on chromosome 12q15. (OMIM)
Galloway-Mowat Syndrome 8  

Exact Synonyms: GAMOS7
Primary IDs: OMIM:618348

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