ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
6 signs/symptoms

Intermediate osteopetrosis

Glycogen storage disease due to LAMP-2 deficiency

CLCN7	(UniProt - OMIM)		LAMP2	(UniProt - OMIM)
PLEKHM1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CLCN7	(0.52)	LAMP2

Citations in the biomedical literature:

Intermediate osteopetrosis		Glycogen storage disease due to LAMP-2 deficiency
	Synonym(s): - Autosomal recessive intermediate osteopetrosis		Synonym(s): - Danon disease - GSD due to LAMP-2 deficiency - Glycogenosis due to LAMP-2 deficiency - Lysosomal glycogen storage disease with normal acid maltase activity

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare cardiac disease - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: any age Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: adult Type of inheritance: x-linked recessive

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

Glycogen storage disease due to LAMP-2 deficiency
	Very frequent - Abnormal gait - Cardiomyopathy / hypertrophic / dilated - Collapse / sudden death / cardiac arrest / cardiorespiratory arrest - Intellectual deficit / mental / psychomotor retardation / learning disability - Muscle weakness / flaccidity - X-linked recessive inheritance
Intermediate osteopetrosis
(no data available)