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Dictionary » HPRT1 deficiency
 

HPRT1 deficiency

Introduction: HPRT1 deficiency

Description of HPRT1 deficiency

HPRT1 deficiency (medical condition): Inherited biochemical disorder of purine metabolism caused by the virtual...more »

See also:

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

HPRT1 deficiency: Related Topics

These medical condition or symptom topics may be relevant to medical information for HPRT1 deficiency:

HPRT1 deficiency: Rare Disease

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

HPRT1 deficiency is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that HPRT1 deficiency, or a subtype of HPRT1 deficiency, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

HPRT1 deficiency as a Disease

HPRT1 deficiency: Another name for Lesch-Nyhan syndrome (or close medical condition association).
  »Introduction: Lesch-Nyhan syndrome
  »Symptoms of Lesch-Nyhan syndrome

HPRT1 deficiency: Related Diseases

HPRT1 deficiency: HPRT1 deficiency is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of HPRT1 deficiency (Lesch-Nyhan syndrome)

Some of the symptoms of HPRT1 deficiency incude:

HPRT1 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 genes. (Source: Genes and Disease by the National Center for Biotechnology)

HPRT1 deficiency: Related Disease Topics

These medical disease topics may be related to HPRT1 deficiency:

Terms associated with HPRT1 deficiency:

Terms Similar to HPRT1 deficiency:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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