Oculopharyngodistal myopathy (disorder)

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April 2020

Congenital ptosis
Digestive system hereditary disorder (disorder)
Disorder of pharynx
Distal muscular dystrophy
Hereditary disorder of the visual system
Pharyngeal paresis

Name: Oculopharyngodistal myopathy (disorder) See more descriptions.

- Oculopharyngodistal myopathy (disorder)
- Oculopharyngeal distal myopathy
- Oculopharyngodistal myopathy
- OPDM - oculopharyngodistal myopathy
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Concept ID: 763829004
Read Codes:
ICD-10 Codes: G710

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