Disease #01071 (ATRX (thalassemia, alpha/mental retardation syndrome (ATRX)), OMIM:301040)

Official abbreviation ATRX
Name thalassemia, alpha/mental retardation syndrome (ATRX)
OMIM ID 301040
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene ATRX
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

3 entries on 1 page. Showing entries 1 - 3.
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00133269 Case 1 - - M ? France - >22y - - - ATRX Osteosarcoma at 9 years ATRX ATRX 1 1 Julien Masliah-Planchon
00133270 Case 2 - - M ? - - 06y - - - ATRX Osteosarcoma ATRX ATRX 1 1 Julien Masliah-Planchon
00381848 184335 - - M no Germany - - - - - ATRX Intellectual disability, Intellectual disability, moderate, Muscular hypotonia, Cerebellar vermis hypoplasia, Dandy-Walker malformation, Microcephaly, Drooling ATRX ATRX 1 1 Andreas Laner
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