Disease #03353 (AGM3 (agammaglobulinemia, type 3, autosomal recessive (AGM3)), OMIM:613501)

Official abbreviation AGM3
Name agammaglobulinemia, type 3, autosomal recessive (AGM3)
OMIM ID 613501
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CD79A
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)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.