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Ontology Browser

Parent Terms Term With Siblings Child Terms
Meckel syndrome 1  
Meckel syndrome 13  
Meckel syndrome 2  
Meckel syndrome 3  
Meckel syndrome 4  
Meckel syndrome 5  
Meckel syndrome 6  
Meckel syndrome 7  
A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of NPHP3 on chromosome 3q22.1. (DO)
Meckel syndrome 8  
Meckel Syndrome, Type 10  
Meckel Syndrome, Type 11  
Meckel Syndrome, Type 12  
Meckel Syndrome, Type 9  
Pancreatic Pseudocyst 
Renal-Hepatic-Pancreatic Dysplasia 1  
Renal-Hepatic-Pancreatic Dysplasia 2  

Exact Synonyms: Goldston syndrome ;   MKS7 ;   Meckel like syndrome ;   Meckel syndrome, type 7 ;   Meckel-Gruber syndrome, type 7 ;   renal hepatic pancreatic dysplasia, Dandy Walker cyst ;   renal-hepatic-pancreatic dysplasia with Dandy-Walker cyst
Primary IDs: MESH:C537756
Alternate IDs: OMIM:267010 ;   RDO:0003651
Xrefs: ORDO:3032
Definition Sources: "DO"

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