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HPRT deficiency

Introduction: HPRT deficiency

Description of HPRT deficiency

HPRT deficiency (medical condition): Inherited biochemical disorder of purine metabolism caused by the...more »

See also:

Lesch-Nyhan syndrome:
  »Introduction: Lesch-Nyhan syndrome
  »Symptoms of Lesch-Nyhan syndrome
  »Tests for Lesch-Nyhan syndrome

HPRT deficiency: Related Topics

These medical condition or symptom topics may be relevant to medical information for HPRT deficiency:

HPRT deficiency: Rare Disease

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

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

HPRT deficiency as a Disease

HPRT deficiency: Another name for Lesch-Nyhan syndrome (or close medical condition association).
  »Introduction: Lesch-Nyhan syndrome
  »Symptoms of Lesch-Nyhan syndrome

HPRT deficiency: Related Diseases

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

Symptoms of HPRT deficiency (Lesch-Nyhan syndrome)

Some of the symptoms of HPRT deficiency incude:

HPRT deficiency: Article Excerpts about Lesch-Nyhan syndrome

Lesch-Nyhan syndrome (LNS) is a rare inherited disease that disrupts the metabolism of the raw material of...(Source: Genes and Disease by the National Center for Biotechnology)

HPRT deficiency: Related Disease Topics

These medical disease topics may be related to HPRT deficiency:

Terms associated with HPRT deficiency:

Terms Similar to HPRT deficiency:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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