Disease #02480 (thalalpa (thalassemia, alpha), OMIM:604131)

Official abbreviation thalalpa
Name thalassemia, alpha
OMIM ID 604131
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 2 genes HBA1, HBA2
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

5 entries on 1 page. Showing entries 1 - 5.
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00433184 Fam3 PubMed: Cadiero 2023 3-generation family, affected father/duaghter/son F;M - Italy - - - - - thalalpa 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) - HBA1, HBA2 1 3 Johan den Dunnen
00433185 Fam4PatI1 PubMed: Cadiero 2023 3-generation family, affected father/son M - Italy - - - - - thalalpa hypochromic and microcytic red blood cells (MCV 70.0 fL, MCH 25.0, 29.5 pg), normal level HbA2 (0.026) - HBA1, HBA2 1 2 Johan den Dunnen
00433186 Fam3PatII1 PubMed: Cadiero 2023 son M - Italy - - - - - thalalpa hypochromic and microcytic red blood cells (MCV 70.0 fL, MCH 25.0, 29.5 pg), increased level HbA2 (0.063) - HBA1, HBA2, HBB 2 1 Johan den Dunnen
00433188 Fam6 PubMed: Cadiero 2023 3-generation family, affected father/daughter/son F;M - Italy - - - - - thalalpa microcytic and hypochromic anemia, with reduced mean corpuscular volume (MCV), and mean corpuscular hemoglobin (MCH), level of HbA2 (0.0027) - HBA1, HBA2 1 3 Johan den Dunnen
00433190 Fam5 PubMed: Cadiero 2023 - F - Italy - - - - - thalalpa microcytic and hypochromic anemia, with normal iron balance, normal HbA2 (0.027), normal HbF (0.003) - HBA1, HBA2 1 1 Johan den Dunnen
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