Disease #00988 (RSSCID (immunodeficiency, severe combined, Athabascan type), OMIM:602450)

Official abbreviation RSSCID
Name immunodeficiency, severe combined, Athabascan type
OMIM ID 602450
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 2 genes DCLRE1C, LIG4
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-11 13:56:28 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00150100 - - - M yes Turkey white 00y04m - - - RSSCID - - DCLRE1C 1 1 Sinem Firtina
00150105 - - - F yes Turkey Turkısh 00y04m - - - RSSCID - DCLRE1C DCLRE1C 1 1 Sinem Firtina
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