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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
progeria +     
Acrogeria, Gottron Type 
Bird Headed Dwarfism Montreal Type 
Congenital Progeroid Syndrome, Petty Type  
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome  
Mandibuloacral Dysplasia 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 
Ruijs-Aalfs syndrome  
Ruvalcaba Churesigaew Myhre Syndrome 
Wiedemann-Rautenstrauch syndrome  

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

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