Disease #00122 (ACEP (aceruloplasminemia), OMIM:604290)

Official abbreviation ACEP
Name aceruloplasminemia
OMIM ID 604290
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 1
Associated with 1 gene CP
Associated tissues -
Disease features -
Remarks -
Date created 2013-04-24 12:32:26 +02:00 (CEST)
Date last edited 2024-12-31 09:44:49 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00001500 - - London aceruloplasminemia family. M no Kenya Indian - - - - ACEP - CERS6 CP 1 2 Alisdair McNeill
00001501 - - - M - Japan Japanese - - - - ACEP - - CP 1 1 Alisdair McNeill
00001502 - - - M no Ireland - - - - - ACEP - - CP 1 1 Alisdair McNeill
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