Disease #07034 (IMD105 (immunodeficiency, type 105, severe combined), OMIM:619924)

Official abbreviation IMD105
Name immunodeficiency, type 105, severe combined
OMIM ID 619924
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PTPRC
Associated tissues -
Disease features -
Remarks -
Date created 2023-10-17 16:07:11 +02:00 (CEST)
Date last edited N/A

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