Disease #04525 (IMD-38 (immunodeficiency, type 38 (IMD-38)), OMIM:616126)

Official abbreviation IMD-38
Name immunodeficiency, type 38 (IMD-38)
OMIM ID 616126
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ISG15
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited N/A