Phenotypes for disease #03019 (immunodeficiency, severe combined, with microcephaly, growth retardation, and sensitivity to ionizing radiation, OMIM:611291)

5 entries on 1 page. Showing entries 1 - 5.
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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     
0000325667 see paper; ..., 18-y died septic shock; microcephaly; growth retardation; chromosomal alterations, urogenital and bone malformations; bacterial and opportunistic infections; autoimmune anemia, thrombocytopenia - - Familial, autosomal recessive 18y - - - - Johan den Dunnen 00435480
0000325668 see paper; ..., 4-y died septic shock; microcephaly; growth retardation; infections bacterial and opportunistic; no autoimmunity - - Familial, autosomal recessive 04y - - - - Johan den Dunnen 00435481
0000325669 see paper; ..., microcephaly; growth retardation; birdlike face, bone malformation; infections bacterial and opportunistic; autoimmune anemia, thrombocytopenia - - Familial, autosomal recessive 14y - - - - Johan den Dunnen 00435482
0000325670 see paper; ..., microcephaly; growth retardation; birdlike face; infections bacterial and opportunistic; no autoimmunity - - Familial, autosomal recessive 3y - - - - Johan den Dunnen 00435483
0000325671 see paper; ..., microcephaly; growth retardation; birdlike face, chromosomal alterations, bone marrow aplasia; recurrent respiratory tract infections; no autoimmunity - - Familial, autosomal recessive 09y - - - - Johan den Dunnen 00435484
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