Phenotypes for disease #01673 (atransferrinemia, OMIM:209300)

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     
0000082783 Severe hypochromic microcytic anemia - - Familial, autosomal recessive - - - - - Mayka Sanchez 00104896
0000082784 Severe hypochromic microcytic anemia - - Familial, autosomal recessive - - - - - Mayka Sanchez 00104897
0000207156 6m, no history of any serious disorder in family; neonatal period severe hypochromic and microcytic anemia with undetectable serum transferrin - - Familial, autosomal recessive 00y08m - - - - Yessine Amri 00269324
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