Disease #02363 (SCIDN (immunodeficiency, severe combined, autosomal recessive, T-cell negative, B-cell negative, NK cell-positive), OMIM:601457)

Official abbreviation SCIDN
Name immunodeficiency, severe combined, autosomal recessive, T-cell negative, B-cell negative, NK cell-positive
OMIM ID 601457
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 8
Phenotype entries for this disease -
Associated with 2 genes RAG1, RAG2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00222863 - - - - - - - - - - - Omenn, SCIDN - RAG1 RAG1 1 1 SIB - Livia Famiglietti
00222864 - - - - - - - - - - - SCIDN - RAG1 RAG1 1 1 SIB - Livia Famiglietti
00222869 - - - - - - - - - - - Omenn, SCIDN - RAG1 RAG1 1 1 SIB - Livia Famiglietti
00222870 - - - - - - - - - - - Omenn, SCIDN - RAG1 RAG1 1 1 SIB - Livia Famiglietti
00222871 - - - - - - - - - - - Omenn, SCIDN - RAG1 RAG1 1 1 SIB - Livia Famiglietti
00222873 - - - - - - - - - - - SCIDN - RAG1 RAG1 1 1 SIB - Livia Famiglietti
00222875 - - - - - - - - - - - Omenn, SCIDN - RAG1 RAG1 1 1 SIB - Livia Famiglietti
00222876 - - - - - - - - - - - SCIDN - RAG1 RAG1 1 1 SIB - Livia Famiglietti
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