Disease #00176 (HDLCD-2 (hypoalphalipoproteinemia (HDL deficiency, type 2 (HDLCD-2))), OMIM:604091)

Official abbreviation HDLCD-2
Name hypoalphalipoproteinemia (HDL deficiency, type 2 (HDLCD-2))
OMIM ID 604091
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 5
Phenotype entries for this disease 0
Associated with 2 genes ABCA1, APOA1
Associated tissues -
Disease features -
Remarks -


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00240084 - - - - - - - - 0 - - HDLCD-2 - LCAT LCAT 1 1 M. Mahdi Motazacker
00240085 - - - - - - - - 0 - - HDLCD-2 - LCAT LCAT 2 1 M. Mahdi Motazacker
00240086 - - - - - Netherlands - - 0 - - HDLCD-2 - LCAT LCAT 1 1 M. Mahdi Motazacker
00240087 - - - - - - - - 0 - - HDLCD-2 - LCAT LCAT 1 1 M. Mahdi Motazacker
00240088 - - - - - Netherlands - - 0 - - HDLCD-2 - LCAT LCAT 1 1 M. Mahdi Motazacker
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