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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Ciliary Motility Disorders +     
Encephalocele +     
Meckel syndrome +     
polycystic kidney disease +     
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 
Ciliary Discoordination due to Random Ciliary Orientation 
Ciliary Dyskinesia with Transposition of Ciliary Microtubules 
Dandy-Walker Malformation with Occipital Cephalocele, Autosomal Dominant 
Daneman Davy Mancer Syndrome 
DK Phocomelia Syndrome 
Fronto-Facio-Nasal Dysplasia 
Hypohidrotic Ectodermal Dysplasia with Hypothyroidism and Ciliary Dyskinesia 
Immotile Cilia Syndrome, due to Defective Radial Spokes 
Immotile Cilia Syndrome, due to Excessively Long Cilia 
Knobloch Syndrome +   
Laryngeal Atresia, Encephalocele, and Limb Deformities 
Meckel syndrome 1  
Meckel Syndrome 10  
Meckel Syndrome 11  
Meckel Syndrome 12  
Meckel syndrome 13  
Meckel Syndrome 14  
Meckel syndrome 2  
Meckel syndrome 3  
A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the TMEM67 gene on chromosome 8q22.1. (DO)
Meckel syndrome 4  
Meckel syndrome 5  
Meckel syndrome 6  
Meckel syndrome 7  
Meckel syndrome 8  
Meckel Syndrome 9  
Meckel-Like Cerebrorenodigital Syndrome 
parietal foramina +   
Podder-Tolmie Syndrome 
Polycystic Kidney, Cataract, and Congenital Blindness 
primary ciliary dyskinesia +   
Sakoda Complex 
Zechi-Ceide Syndrome 

Synonyms
Exact Synonyms: MKS3 ;   Meckel syndrome type 3 ;   Meckel-Gruber Syndrome, Type 3
Primary IDs: MESH:C536132
Alternate IDs: OMIM:607361
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/16415887 "DO" "DO"

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