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Dictionary » Smith-Lemli-Opitz syndrome, type I

Smith-Lemli-Opitz syndrome, type I

Smith-Lemli-Opitz syndrome, type I: Related Topics

These medical condition or symptom topics may be relevant to medical information for Smith-Lemli-Opitz syndrome, type I:

Smith-Lemli-Opitz syndrome, type I: Rare Disease

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

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

Terms associated with Smith-Lemli-Opitz syndrome, type I:

Terms Similar to Smith-Lemli-Opitz syndrome, type I:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

  • Association mechanism
  • Association of cutaneous vascular malformations and different pigmentary disorders
  • Association of muscular pseudohypertrophy and hypothyroidism in children
  • Association of partial sacral agenesis with intact first sacral vertebra ('sickle-shaped sacrum'), a presacral mass, and anorectal malformation
  • Association of skeletal defects resembling achondrogenesis with generalized bone sclerosis
  • Association of tetra-amelia, ectodermal dysplasia, hypoplastic lacrimal ducts and sacs opening towards the exterior, peculiar face, and developmental
  • Association system
  • Association test
  • Association time
  • Association tract
  • Associationism

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