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Meckel syndrome 6 (DOID:0070120)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1)
Parent Terms Term With Siblings Child Terms
Encephalocele +     
Meckel syndrome +     
Arima Syndrome 
autosomal dominant polycystic kidney disease +   
autosomal recessive polycystic kidney disease +   
Cerebellar Vermis Aplasia with Associated Features suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome 
Cerebrorenodigital Syndrome with Limb Malformations and Triradiate Acetabula 
Dandy-Walker Malformation with Occipital Cephalocele, Autosomal Dominant 
Daneman Davy Mancer Syndrome 
DK Phocomelia Syndrome 
Fronto-Facio-Nasal Dysplasia 
Knobloch Syndrome  
Knobloch Syndrome Type II 
Knobloch Syndrome Type III 
Laryngeal Atresia, Encephalocele, and Limb Deformities 
Meckel syndrome 1  
Meckel syndrome 13  
Meckel syndrome 2  
Meckel syndrome 3  
Meckel syndrome 4  
Meckel syndrome 5  
Meckel syndrome 6  
A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of CC2D2A on chromosome 4p15.32. (DO)
Meckel syndrome 7  
Meckel syndrome 8  
Meckel Syndrome, Type 10  
Meckel Syndrome, Type 11  
Meckel Syndrome, Type 12  
Meckel Syndrome, Type 9  
Meckel-Like Cerebrorenodigital Syndrome 
parietal foramina +   
Podder-Tolmie Syndrome 
Polycystic Kidney Disease, Type 1  
Polycystic Kidney, Cataract, and Congenital Blindness 
Sakoda Complex 
Zechi-Ceide Syndrome 

Exact Synonyms: MKS6 ;   Meckel Syndrome, Type 6 ;   Meckel-Gruber syndrome, type 6
Primary IDs: MESH:C567365
Alternate IDs: DOID:9000346 ;   OMIM:612284 ;   RDO:0015456
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/18513680

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