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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Joubert syndrome +     
nephronophthisis +     
Joubert syndrome 1  
Joubert syndrome 10  
Joubert Syndrome 12  
Joubert Syndrome 13  
Joubert syndrome 14  
Joubert syndrome 15  
Joubert Syndrome 16  
Joubert Syndrome 17  
Joubert Syndrome 18  
Joubert Syndrome 2  
Joubert syndrome 20  
Joubert syndrome 21  
Joubert syndrome 22  
Joubert syndrome 23  
Joubert syndrome 24  
Joubert syndrome 25  
Joubert Syndrome 26  
Joubert Syndrome 27  
Joubert Syndrome 28  
Joubert syndrome 29 
Joubert syndrome 3  
Joubert syndrome 30  
Joubert syndrome 31  
Joubert syndrome 32  
Joubert syndrome 33  
JOUBERT SYNDROME 35  
Joubert Syndrome 36  
Joubert Syndrome 37  
Joubert Syndrome 38  
Joubert Syndrome 39  
Joubert syndrome 4  
Joubert Syndrome 40  
Joubert syndrome 5  
Joubert syndrome 6  
Joubert syndrome 7  
Joubert syndrome 8  
Joubert syndrome 9  
Joubert syndrome with orofaciodigital defect  
Meckel Syndrome 10  
nephronophthisis 1  
nephronophthisis 11  
nephronophthisis 12  
A nephronophthisis that has_material_basis_in homozygous or compound heterozygous mutation in the TTC21B gene on chromosome 2q24. (DO)
nephronophthisis 13  
nephronophthisis 14  
nephronophthisis 15  
nephronophthisis 16  
nephronophthisis 18  
nephronophthisis 19  
nephronophthisis 2  
nephronophthisis 20  
nephronophthisis 3  
nephronophthisis 4  
nephronophthisis 7  
nephronophthisis 9  
nephronophthisis-like nephropathy 1  
Nephronophthisis-like Nephropathy 2  

Synonyms
Exact Synonyms: NPHP12
Narrow Synonyms: JBTS11 ;   JOUBERT SYNDROME 11
Broad Synonyms: TTC21B-RELATED DISORDER
Primary IDs: MIM:613820
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/21258341 "DO" "DO"

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