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Dictionary » OPPG
 

OPPG

Introduction: OPPG

Description of OPPG

OPPG (medical condition): A rare genetic disorder characterized by early onset of osteoporosis (during...more »

See also:

Osteoporosis-pseudoglioma syndrome:
  »Introduction: Osteoporosis-pseudoglioma syndrome
  »Symptoms of Osteoporosis-pseudoglioma syndrome

OPPG: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

OPPG is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that OPPG, or a subtype of OPPG, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list OPPG as a "rare disease".

Source - Orphanet

OPPG as a Disease

OPPG: Another name for Osteoporosis-pseudoglioma syndrome (or close medical condition association).
  »Introduction: Osteoporosis-pseudoglioma syndrome
  »Symptoms of Osteoporosis-pseudoglioma syndrome

OPPG: Related Diseases

OPPG: OPPG is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of OPPG (Osteoporosis-pseudoglioma syndrome)

Some of the symptoms of OPPG incude:

OPPG: Related Disease Topics

These medical disease topics may be related to OPPG:

Terms associated with OPPG:

Terms Similar to OPPG:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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