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Ontology Browser

Term:
Joubert syndrome with orofaciodigital defect (DOID:0060376)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Joubert syndrome +     
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 4  
Joubert syndrome 5  
Joubert syndrome 6  
Joubert syndrome 7  
Joubert syndrome 8  
Joubert syndrome 9  
Joubert syndrome with orofaciodigital defect  
A Joubert syndrome that is characterized by orofaciodigital defect. (DO)
Juberg Hayward Syndrome  
Meckel Syndrome, Type 10  
Mohr Syndrome  
nephronophthisis 12  
nephronophthisis 14  
Orofaciodigital Syndrome 12 
Orofaciodigital Syndrome 13 
orofaciodigital syndrome I  
orofaciodigital syndrome III  
orofaciodigital syndrome IV  
orofaciodigital syndrome IX  
orofaciodigital syndrome V  
orofaciodigital syndrome VII 
orofaciodigital syndrome VIII 
orofaciodigital syndrome X 
orofaciodigital syndrome XI 
Orofaciodigital Syndrome XIV  
Orofaciodigital Syndrome XV  
orofaciodigital syndrome XVI  
orofaciodigital syndrome XVII  
Orofaciodigital Syndrome XVIII  

Synonyms
Exact Synonyms: OFD6 ;   OFDS VI ;   Oral-Facial-Digital Syndrome, Type VI ;   Oral-facial-digital syndrome, type 6 ;   Orofaciodigital Syndrome VI ;   Orofaciodigital syndrome 6 ;   Polydactyly cleft lip palate psychomotor retardation ;   Polydactyly, Cleft Lip-Palate or Lingual Lump, and Psychomotor Retardation ;   Varadi Papp syndrome ;   Varadi Syndrome
Primary IDs: MESH:C536531 ;   RDO:0002142
Alternate IDs: OMIM:277170
Xrefs: GARD:4412 ;   NCI:C124841 ;   ORDO:2754
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/23716954 "DO"

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