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
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