Disease #06300 (IMD52 (Immunodeficiency, type 52), OMIM:617514)

Official abbreviation IMD52
Name Immunodeficiency, type 52
OMIM ID 617514
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene LAT
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited 2022-05-23 16:58:44 +02:00 (CEST)

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