OPD 2 syndrome (medical condition): A rare genetic disorder characterized by head, face, mouth and bone abnormalities.
See also:
Oto-palato-digital syndrome, type 2:
»Introduction: Oto-palato-digital syndrome, type 2
»Symptoms of Oto-palato-digital syndrome, type 2
OPD 2 syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that OPD 2 syndrome, or a subtype of OPD 2 syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
OPD 2 syndrome: Another name for Oto-palato-digital syndrome, type 2 (or close medical condition association).
»Introduction: Oto-palato-digital syndrome, type 2
»Symptoms of Oto-palato-digital syndrome, type 2
Some of the symptoms of OPD 2 syndrome incude:
See full list of 56 symptoms of OPD 2 syndrome (Oto-palato-digital syndrome, type 2)
These medical disease topics may be related to OPD 2 syndrome:
Source - NIH
Search to find out more about OPD 2 syndrome:
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