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Ontology Browser

Premature Aging Syndrome, Okamoto Type (DOID:9002463)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
progeria +     
Acrogeria, Gottron Type 
Bird Headed Dwarfism Montreal Type 
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome  
Neonatal Progeroid Syndrome  
Penttinen-Aula Syndrome  
Petty Laxova Wiedemann Syndrome 
Premature Aging Syndrome, Okamoto Type 
Progeria Short Stature Pigmented Nevi 
Progeria Syndrome, Childhood-Onset +   
Progeroid Facial Appearance with Hand Anomalies 
Progeroid Syndrome, Congenital, Petty Type  
Ruijs-Aalfs syndrome  
Ruvalcaba Churesigaew Myhre Syndrome 

Primary IDs: MESH:C566621
Alternate IDs: OMIM:601811

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