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Dictionary » IGDA syndrome
 

IGDA syndrome

Introduction: IGDA syndrome

Description of IGDA syndrome

IGDA syndrome (medical condition): A rare genetic eye disorder involving glaucoma and iris anomalies and...more »

See also:

Iridogoniodysgenesis type1:
  »Introduction: Iridogoniodysgenesis type1
  »Symptoms of Iridogoniodysgenesis type1

IGDA syndrome: Related Topics

These medical condition or symptom topics may be relevant to medical information for IGDA syndrome:

IGDA syndrome: Rare Disease

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

IGDA syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that IGDA syndrome, or a subtype of IGDA syndrome, 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 IGDA syndrome as a "rare disease".

Source - Orphanet

IGDA syndrome as a Disease

IGDA syndrome: Another name for Iridogoniodysgenesis type1 (or close medical condition association).
  »Introduction: Iridogoniodysgenesis type1
  »Symptoms of Iridogoniodysgenesis type1

IGDA syndrome: Related Diseases

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

Symptoms of IGDA syndrome (Iridogoniodysgenesis type1)

Some of the symptoms of IGDA syndrome incude:

Terms associated with IGDA syndrome:

Terms Similar to IGDA syndrome:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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