GTPCH deficiency

Introduction: GTPCH deficiency

Description of GTPCH deficiency

GTPCH deficiency (medical condition): A rare metabolic disorder caused by an enzyme...more »

See also:

GTP cyclohydrolase deficiency:
  »Introduction: GTP cyclohydrolase deficiency
  »Symptoms of GTP cyclohydrolase deficiency

GTPCH deficiency: Related Topics

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

• Deficiency
• Deficiency disease

GTPCH deficiency: Rare Disease

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list GTPCH deficiency as a "rare disease".

Source - Orphanet

GTPCH deficiency as a Disease

GTPCH deficiency: Another name for GTP cyclohydrolase deficiency (or close medical condition association).
  »Introduction: GTP cyclohydrolase deficiency
  »Symptoms of GTP cyclohydrolase deficiency

GTPCH deficiency: Related Diseases

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

• Genetic conditions
• Metabolic conditions
• Congenital conditions - metabolic disorders
• Congenital conditions

Symptoms of GTPCH deficiency (GTP cyclohydrolase deficiency)

Some of the symptoms of GTPCH deficiency incude:

• Increased blood phenylalanine levels
• GTP cyclohydrolase deficiency
• Increased urine phenylketone level
• Neurological signs
• Psychomotor retardation

See full list of 17 symptoms of GTPCH deficiency (GTP cyclohydrolase deficiency)

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Medical dictionaries:

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• Medical Acronymns/Abbreviations

More Medical Dictionary Topics

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