Disease #05465 (del 22q11.2 (chromosome deletion syndrome 22q11.2, distal), OMIM:611867)

Official abbreviation del 22q11.2
Name chromosome deletion syndrome 22q11.2, distal
OMIM ID 611867
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 0 genes -
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Disease features -
Remarks -
Date created 2018-08-04 00:00:12 +02:00 (CEST)
Date last edited 2022-09-08 15:28:52 +02:00 (CEST)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00173998 - PubMed: Beddow RA 2011 - M - - - - - - - del 22q11.2, RTPS1 , it SMARCB1 SMARCB1 1 1 Julia Lopez
00173999 - PubMed: Lafay-Cousin L 2009 - M - - - - - - - del 22q11.2, RTPS1 , st SMARCB1 SMARCB1 1 1 Julia Lopez
00174115 - PubMed: Toth G 2011 - - - - - - - - - del 22q11.2 Malignant rhabdoid tumor of the soft tissue (MRT) / at birth SMARCB1 SMARCB1 1 1 Julia Lopez
00174253 - PubMed: Wieser R 2005 - M - - - - - - - del 22q11.2 RTK: kidney SMARCB1 SMARCB1 1 1 Julia Lopez
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