Details of Disease | DrugMAP

General Information of Disease (ID: DISUG070)

Disease Name	Hypoalphalipoproteinemia, primary, 2
Synonyms	High Density Lipoprotein Deficiency; Apolipoprotein A-I Deficiency; ApoA-I and apoC-III deficiency, combined; hypoalphalipoproteinemia, primary, 2, with or without corneal clouding; HYPOALPHALIPOPROTEINEMIA, PRIMARY, 2
Disease Hierarchy	DISYKSRF: Genetic disease DISUG070: Hypoalphalipoproteinemia, primary, 2
Disease Identifiers	MONDO ID MONDO_0032766 UMLS CUI C5551172 OMIM ID 618463 MedGen ID 1789263

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
APOA1	TT7GN3U	Strong	Autosomal recessive	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
APOA1	OT5THARI	Strong	Autosomal recessive	[1]
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References

1	A novel ApoA-I truncation (ApoA-IMytilene) associated with decreased ApoA-I production. Atherosclerosis. 2014 Aug;235(2):470-6. doi: 10.1016/j.atherosclerosis.2014.05.935. Epub 2014 Jun 2.