Disease #03116 (HACD59 (anemia, hemolytic, CD59-mediated, with/without immune-mediated polyneuropathy (HACD-59)), OMIM:612300)

Official abbreviation HACD59
Name anemia, hemolytic, CD59-mediated, with/without immune-mediated polyneuropathy (HACD-59)
OMIM ID 612300
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene CD59
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00081002 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - HACD59 Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy (OMIM:612300) CD59 CD59 1 1 Daniel Trujillano
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