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Dictionary » CIID


Introduction: CIID

Description of CIID

CIID (medical condition): A very rare, recessively inherited syndrome characterized mainly by a weak...more »

See also:

ICF syndrome:
  »Introduction: ICF syndrome
  »Symptoms of ICF syndrome
  »Treatments for ICF syndrome

CIID: Rare Disease

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

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

CIID as a Disease

CIID: Another name for ICF syndrome (or close medical condition association).
  »Introduction: ICF syndrome
  »Symptoms of ICF syndrome
  »Treatments for ICF syndrome

CIID: Related Diseases

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

Causes of CIID

Some of the causes of CIID are included in the list below:

Symptoms of CIID (ICF syndrome)

Some of the symptoms of CIID incude:

Treatments for CIID (ICF syndrome)

Treatments for CIID (ICF syndrome) include:

  • Repeated immunoglogulin infusions
  • Vitamin A - possibly used for related vitamin A deficiency

Treatment of CIID: For more treatment information about CIID, see treatment of ICF syndrome (CIID)

Terms associated with CIID:

Terms Similar to CIID:

Source - NIH

Interesting Medical Articles:

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  • Monosomy 1p36 syndrome
  • Monosomy 1q
  • Monosomy 1q, proximal
  • Monosomy 1q, terminal

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