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Diseases

Danon Disease

danon disease

Entity Type
Diseases
Relation Groups
1
Relation Preview
7

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Danon Disease
Standard Disease Name
danon disease
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D052120
OMIM ID
300257
UMLS ID
C0878677
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:A genetic metabolic disorder causing hypertrophic cardiomyopathy. Mutations of the LAMP2 gene have been reported in association with this disease.|MSH2017_2016_08_12:An X-linked dominant multisystem disorder resulting in cardiomyopathy, myopathy and INTELLECTUAL DISABILITY. It is caused by mutation in the gene encoding LYSOSOMAL-ASSOCIATED MEMBRANE PROTEIN 2.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease7 Targets
03
MPP2
membrane palmitoylated protein 2
membrane palmitoylated protein 2
07
VPS4A
vacuolar protein sorting 4 homolog A
vacuolar protein sorting 4 homolog A