Disease #00988 (Severe combined immunodeficiency with sensitivity to ionizing radiation, OMIM:602450)

Official abbreviation -
Name Severe combined immunodeficiency with sensitivity to ionizing radiation
OMIM ID 602450
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 2 genes DCLRE1C, LIG4
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Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00150100 - - - M yes Turkey white 00y04m 0 - - Severe combined immunodeficiency with sensitivity to ionizing radiation - - DCLRE1C 1 1 Sinem Firtina
00150105 - - - F yes Turkey Turkısh 00y04m 0 - - Severe combined immunodeficiency with sensitivity to ionizing radiation - DCLRE1C DCLRE1C 1 1 Sinem Firtina
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