Disease association ontology term - MONDO:0010457 - Ogden syndrome
Term summary
- ID
- MONDO:0010457
- Name
- Ogden syndrome
- Ontology or CV name
- Disease association
- Definition
- Ogden syndrome is a rare, genetic progeroid syndrome characterized by a variable phenotype including postnatal growth delay, severe global developmental delay, hypotonia, non-specific dysmorphic facies with aged appearance and cryptorchidism, as well as cardiac arrthymias and skeletal anomalies. Patients typically present with widely opened fontanels, mainly truncal hypotonia, a waddling gait with hypertonia of the extremities, small hands and feet, broad great toes, scoliosis and redundant skin with lack of subcutaneous fat.
