Phenotypes for disease #01071 (ATRX (thalassemia, alpha/mental retardation syndrome (ATRX)), OMIM:301040)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000106016 Osteosarcoma at 9 years - - Familial, X-linked - - - - - Julien Masliah-Planchon 00133269
0000106017 Osteosarcoma - - Unknown - - - - - Julien Masliah-Planchon 00133270
0000275690 Intellectual disability, Intellectual disability, moderate, Muscular hypotonia, Cerebellar vermis hypoplasia, Dandy-Walker malformation, Microcephaly, Drooling - - Familial, X-linked recessive - 11y - - - Andreas Laner 00381848
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