Phenotypes for disease #02480 (thalalpa (thalassemia, alpha), OMIM:604131)

6 entries on 1 page. Showing entries 1 - 6.
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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     
0000323716 reduction in the MCV (range of 63.0–67.0 fL) and MCH (range of 20.1–20.9 pg), with normal levels of HbA2 (0.025) alpha thalassemia - Familial, autosomal recessive - - - - - Johan den Dunnen 00433184
0000323717 hypochromic and microcytic red blood cells (MCV 70.0 fL, MCH 25.0, 29.5 pg), normal level HbA2 (0.026) alpha thalassemia - Familial, autosomal recessive - - - - - Johan den Dunnen 00433185
0000323718 hypochromic and microcytic red blood cells (MCV 70.0 fL, MCH 25.0, 29.5 pg), increased level HbA2 (0.063) alpha thalassemia - Familial, autosomal recessive - - - - - Johan den Dunnen 00433186
0000323720 microcytic and hypochromic anemia, with reduced mean corpuscular volume (MCV), and mean corpuscular hemoglobin (MCH), level of HbA2 (0.0027) alpha thalassemia - Familial, autosomal recessive - - - - - Johan den Dunnen 00433188
0000323722 microcytic and hypochromic anemia, with normal iron balance, normal HbA2 (0.027), normal HbF (0.003) alpha thalassemia - Unknown - - - - - Johan den Dunnen 00433190
0000337849 see paper; ..., Hb Bart's during neonatal screening; microcytic/hypochromic anemia, mild reticulocytosis Hb Bart's (neonatal screening) alpha thalassemia Familial, autosomal recessive - - - - - Johan den Dunnen 00448672
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