ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
6 signs/symptoms

Pseudohypoaldosteronism type 2E

Glycogen storage disease due to muscle phosphofructokinase deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CUL3	(0.63)	PFKM

Citations in the biomedical literature:

Pseudohypoaldosteronism type 2E		Glycogen storage disease due to muscle phosphofructokinase deficiency
	Synonym(s): - PHA2E		Synonym(s): - GSD due to muscle phosphofructokinase deficiency - GSD type 7 - Glycogen storage disease type 7 - Glycogenosis due to muscle phosphofructokinase deficiency - Glycogenosis type 7 - Tarui disease

	Classification (Orphanet): - Rare circulatory system disease - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare hematologic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the circulatory system -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - No MeSH references

Glycogen storage disease due to muscle phosphofructokinase deficiency
	Very frequent - Anaemia - Autosomal recessive inheritance - Metabolic anomalies - Myotonia Frequent - Hyperuricemia - Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy
Pseudohypoaldosteronism type 2E
(no data available)