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Dictionary » Familial middle ear ossicular anomalies
 

Familial middle ear ossicular anomalies

Introduction: Familial middle ear ossicular anomalies

Description of Familial middle ear ossicular anomalies

Familial middle ear ossicular anomalies (medical condition): A familial form of conductive deafness caused by an abnormal small...more »

See also:

Ossicular Malformations, familial:
  »Introduction: Ossicular Malformations, familial
  »Symptoms of Ossicular Malformations, familial

Familial middle ear ossicular anomalies: Related Topics

These medical condition or symptom topics may be relevant to medical information for Familial middle ear ossicular anomalies:

Familial middle ear ossicular anomalies: Rare Disease

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

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

Familial middle ear ossicular anomalies as a Disease

Familial middle ear ossicular anomalies: Another name for Ossicular Malformations, familial (or close medical condition association).
  »Introduction: Ossicular Malformations, familial
  »Symptoms of Ossicular Malformations, familial

Familial middle ear ossicular anomalies: Related Diseases

Familial middle ear ossicular anomalies: Familial middle ear ossicular anomalies is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Familial middle ear ossicular anomalies (Ossicular Malformations, familial)

Some of the symptoms of Familial middle ear ossicular anomalies incude:

Terms associated with Familial middle ear ossicular anomalies:

Terms Similar to Familial middle ear ossicular anomalies:

Source - NIH

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