Disease #03207 (AHUS5 (hemolyticuremic syndrome, atypical, susceptibility type 5 (AHUS5)), OMIM:612925)

Official abbreviation AHUS5
Name hemolyticuremic syndrome, atypical, susceptibility type 5 (AHUS5)
OMIM ID 612925
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene C3
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2022-01-07 11:58:28 +01:00 (CET)

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