Disease #06310 (IMD58 (Immunodeficiency 58), OMIM:618131)

Official abbreviation IMD58
Name Immunodeficiency 58
OMIM ID 618131
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene RLTPR
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A

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