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Ontology Browser
Term:
Prader-Willi Habitus, Osteopenia, and Camptodactyly (DOID:9005814)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0) Naked Mole-rat: (0) Green Monkey: (0)
Parent Terms Term With Siblings Child Terms
osteoporosis +     
Prader-Willi syndrome +     
Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis 
Diabetic Bone Disease 
Female Athlete Triad Syndrome 
glucocorticoid-induced osteoporosis 
Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy 
Hernandez Fragoso Syndrome 
hypophosphatemic nephrolithiasis/osteoporosis +   
idiopathic juvenile osteoporosis  
Infantile Multisystem Neurologic Disease with Osseous Fragility 
Macroepiphyseal Dysplasia, McAlister Coe Type 
Osteoporosis, Childhood- or Juvenile-Onset, with Developmental Delay  
Postmenopausal Osteoporosis  
Prader-Willi Habitus, Osteopenia, and Camptodactyly 
Prader-Willi-Like Syndrome Associated with Chromosome 6 
Premature Aging, Okamoto Type 
Schaaf-Yang syndrome  
Singleton Merten Syndrome +   
Winchester syndrome  

Synonyms
Exact Synonyms: Urban Rogers Meyer syndrome
Primary IDs: MESH:C538276
Alternate IDs: OMIM:264010

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